http://pharmaboard.com/ Protechpharma ® Career Network, LLC Protechpharma ® Career Network, LLC | Talent and Opportunities | Growth and Success | Protechpharma Connects them All! en-us RSS-Writer-2010-05-16 bob@protechpharma.com (Website Administrator) bob@protechpharma.com (Website Administrator) 2018-01-23MST11:10:46-25200 Tue, 23 Jan 2018 11:10:46 America/Denver 2018 Pharmaboard&reg; by Protechpharma&reg | Talent and Opportunities | Growth and Success | Pharmaboard&reg; Connects them All! http://pharmaboard.com/ http://pharmaboard.com/images/logo-2012.png Pharmaboard&reg; by Protechpharma&reg | Talent and Opportunities | Growth and Success | Pharmaboard&reg; Connects them All! MODULEDESCRIPTION Manager Environmental Health & Safety <b>Experience:</b> 8 Year(s)<br/><b>Location:</b> New York<br/><b>Industry Type:</b> Rx: Solid Dose / Tablets / Capsules<br/><b>Summary:</b> <table width="849"> <tbody> <tr> <td colspan="3" width="717"> <p> Bachelor&#39;s degree from a four-year college or university in an Engineering, Health Sciences or Environmental Sciences discipline.</p> <p> &sect;&nbsp; Minimum of 8 years&rsquo; related experience and/or training, or equivalent combination of education and experience.</p> </td> </tr> <tr> <td rowspan="2" width="132"> <br /> <p> Knowledge</p> </td> <td colspan="3" width="717"> <p> <em>Proficiency in a body of information required for the job&nbsp;&nbsp;&nbsp; </em></p> <p> <em>e.g. knowledge of FDA regulations, GMP/GLP/GCP, Lean Manufacturing, Six-Sigma, etc.</em></p> </td> </tr> <tr> <td colspan="3" width="717"> <p> &sect;&nbsp; Thorough knowledge of current Federal, State and Local safety/environmental rules and regulations.</p> <p> &sect;&nbsp; Ability to apply concepts of basic algebra and geometry.&nbsp; Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations.</p> </td> </tr> <tr> <td rowspan="2" width="132"> <p> Skills</p> <p> &amp;</p> <p> Abilities</p> </td> <td colspan="3" width="717"> <p> <em>Often referred to as &ldquo;competencies&rdquo;, leadership attributes, skills, abilities or behaviors that may be enterprise, functional or job specific&nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp;e.g. coaching, negotiation, calibration, technical writing</em> <em>etc.</em></p> </td> </tr> <tr> <td colspan="3" width="717"> <p> &sect;&nbsp; Skilled in Excel Spreadsheet software and MS Office Suite Word Processing software.</p> <p> &sect;&nbsp; Ability to calculate figures and amounts such as discounts, interest, commissions, proportions, percentages, area, circumference, and volume.&nbsp;</p> <p> &sect;&nbsp; Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form.&nbsp;</p> <p> &sect;&nbsp; Ability to deal with problems involving several concrete variables in standardized situations.</p> <p> &sect;&nbsp; Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.&nbsp; Ability to write routine reports and correspondence.&nbsp;</p> <p> &sect;&nbsp; Ability to speak effectively before groups of customers or employees of organization.</p> <p> &sect;&nbsp; Technical Skills - Assesses own strengths and weaknesses; Pursues training and development opportunities; Strives to continuously build knowledge and skills; Shares expertise with others.</p> <p> &sect;&nbsp; Quality Management - Looks for ways to improve and promote quality; Demonstrates accuracy and thoroughness.</p> <p> &sect;&nbsp; Planning/Organizing - Prioritizes and plans work activities; Uses time efficiently; Plans for additional resources; Sets goals and objectives; Organizes or schedules other people and their tasks; Develops realistic action plans.</p> <p> &sect;&nbsp; Adaptability - Adapts to changes in the work environment; Manages competing demands; Changes approach or method to best fit the situation; Able to deal with frequent change, delays, or unexpected events.</p> <p> &sect;&nbsp; Initiative - Volunteers readily; Undertakes self-development activities; Seeks increased responsibilities; Takes independent actions and calculated risks; Looks for and takes advantage of opportunities; Asks for and offers help when needed.</p> </td> </tr> <tr> <td rowspan="2" width="132"> <p> Physical Requirements</p> </td> <td colspan="3" width="717"> <p> <em>Physical &amp; mental requirements&nbsp;&nbsp;&nbsp;&nbsp; e.g. lift 40 pounds, walk across plant/warehouse, business travel (% of time), driving as part of work responsibilities, etc.</em></p> </td> </tr> <tr> <td colspan="3" width="717"> <p> &sect;&nbsp; While performing the duties of this job, the employee is occasionally required to climb or balance and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 50 pounds.</p> </td> </tr> <tr> <td colspan="4" width="849"> <p> &nbsp;</p> </td> </tr> </tbody> </table> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=781 http://pharmaboard.com/empid=781 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Associate Director National Accounts <b>Experience:</b> 5 Year(s)<br/><b>Location:</b> New Jersey<br/><b>Industry Type:</b> Rx: Solid Dose / Tablets / Capsules<br/><b>Summary:</b> <div class="full_content"> <div class="main_content_box" id="description_box"> <div class="job_description"> <p style="MARGIN-BOTTOM: 0px; MARGIN-TOP: 0px"> &nbsp;</p> <div class="job_qualifications"> <div> <font color="#565656" face="Arial" size="2"><b><i><font color="#565656" face="Arial" size="2"><b><i><font color="#565656" face="Arial" size="2">Requirements</font></i></b></font></i></b> </font> <div> <font color="#565656" face="Arial" size="2">&nbsp;</font></div> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">The following listed requirements need to be met at a minimum level to be considered for the job:</font></font></div> <ul> <li> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">At least 5 years of sales management and GPO/IDN experience in health care</font></font></div> </li> <li> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">Experience with Microsoft Office applications including: Word, Excel, PowerPoint, &amp; Outlook</font></font></div> </li> </ul> <div> <font color="#565656" face="Arial" size="2"><b><i><font color="#565656" face="Arial" size="2">Preferred Skills/Qualification</font></i></b></font></div> <div> <font color="#565656" face="Arial" size="2">&nbsp;</font></div> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">The below skills are attributes that may not be mandatory, but are definitely desired in the ideal candidate.</font></font></div> <ul> <li> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">Experience National Account Strategic Plans</font></font></div> </li> <li> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">Experience with business strategy and key drivers for effective training programs</font></font></div> </li> <li> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">Experience with health care industry sales</font></font></div> </li> <li> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">Experience with negotiating contracts</font></font></div> </li> <li> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">Demonstrated track record of sales success</font></font></div> </li> <li> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">Demonstrated management, coaching and interpersonal skills</font></font></div> </li> <li> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">Demonstrated presentation and communication skills</font></font></div> </li> <li> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">Ability to understand and communicate economic and clinical information</font></font></div> </li> <li> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">Ability to develop and maintain senior account relationships</font></font></div> </li> <li> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">Ability to work cross-functionally to achieve business goals</font></font></div> </li> <li> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">Ability to help set goals and strategic objectives, then balance short-term goals with a strategic vision</font></font></div> </li> <li> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">Ability to travel 50-75%</font></font></div> </li> <li> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">Ability to maintain confidentiality and exercise discretion in business relationships</font></font></div> </li> <li> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">At least 3 years&rsquo; experience in medical device sales with GPO/IDN responsibility</font></font></div> </li> <li> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">At least 10 years of sales experience</font></font></div> </li> </ul> <div> <font color="#565656" face="Arial" size="2"><b><i><font color="#565656" face="Arial" size="2">Education:</font></i></b></font></div> <ul> <li> <div> <font color="#565656" face="Arial" size="2"><font color="#565656" face="Arial" size="2">Bachelor&rsquo;s Degree in Business or related field</font></font></div> </li> </ul> </div> </div> </div> </div> </div> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=780 http://pharmaboard.com/empid=780 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Senior Manager, R&D Quality <b>Experience:</b> 5 Year(s)<br/><b>Location:</b> California<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <div> <b><font color="#565656" face="Verdana" size="2">Minimum Requirements:</font></b></div> <ul> <li> <div align="left"> <font size="2">Demonstrated knowledge of Computer System Validation in a global GxP environment</font></div> </li> <li> <div align="left"> <font size="2">General understanding of preclinical, clinical, pharmacovigilance, and manufacturing processes and systems.</font></div> </li> <li> <div align="left"> <font size="2">Experience in CSV auditing in a global GxP environment; In depth understanding of preclinical, clinical, pharmacovigilance, and manufacturing processes and systems</font></div> </li> <li> <div align="left"> <font size="2">Operational experience in a GLP, GCP, PV, GMP, CSV QA, or CSV IT capacity will be considered.</font></div> </li> <li> <font face="Arial" size="2">Extensive knowledge of global regulatory requirements.</font></li> <li> <font face="Arial" size="2">Knowledge/understanding of the approach and perspectives of regulatory agencies.</font></li> <li> <font face="Arial" size="2">Ability to ensure strategic risk focus and prioritize activities in response to the myriad of complex, inconsistent, and constantly evolving global regulations and expectations.</font></li> <li> <font face="Arial" size="2">Excellent written and verbal communication skills including presentation skills.</font></li> </ul> <div align="left"> <font size="2"><font face="Arial">&nbsp;</font><b><font color="#565656" face="Verdana">Education:&nbsp;</font></b></font></div> <ul> <li> <font size="2"><b><font color="#565656" face="Verdana">&nbsp;</font></b>Bachelor&rsquo;s degree (BA/BS) degree in a Technical Discipline (Life Sciences, Computer Science, Engineering, etc.)</font></li> <li> <div align="left"> <font size="2"><i>Preferred Education</i>: Advanced degree (MS/PhD) in a Technical Discipline (Life Sciences, Computer Science, Engineering, JD, MD, etc.)</font></div> </li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=779 http://pharmaboard.com/empid=779 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Sr Account Specialist - Health Systems Management <b>Experience:</b> 7 Year(s)<br/><b>Location:</b> Washington<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <div> <div id="description_box"> <div> <div> <p> &nbsp;</p> <p> <strong>Education:</strong></p> <p> &nbsp;</p> <ul> <li> Bachelor&rsquo;s Degree or higher is required</li> </ul> <p> &nbsp;</p> <p> <strong>Requirements:</strong></p> <p> &nbsp;</p> <ul> <li> Minimum seven years total pharmaceutical or medical device experience</li> <li> Minimum five years sales and/or reimbursement experience</li> <li> Knowledge of the Academic Medical Center/hospital environment</li> </ul> <p> &nbsp;</p> <p> <strong>Preferred Skills / Qualifications</strong>:</p> <p> &nbsp;</p> <ul> <li> Knowledge and experience of legal and regulatory compliance requirements related to the Pharma/Biotech</li> <li> Proven track record with documentation of successful sales performance</li> <li> Neurological sales background preferred</li> <li> Excellent interpersonal skills to effectively work with many diverse customers</li> <li> Strong organizational, analytical and business planning skills</li> <li> Excellent written and verbal communication skills. Must be able to communicate with many diverse customer audiences, therapeutic decision makers, and other influencers</li> <li> Strong problem resolution skills</li> <li> Financial/budgetary experience</li> <li> Experience with physician administered injectables preferred within a buy &amp; bill Medicare Part B/Medical benefit environment or other comparable reimbursement experiences</li> <li> Ability to travel adequately to cover territory, as well as overnight attendance at training meetings</li> <li> Ability to pass a pre-employment drug screening test</li> </ul> <p> &nbsp;</p> </div> </div> </div> </div> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=778 http://pharmaboard.com/empid=778 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Assoc. Dir., Procurement (of Mktg Services) <b>Experience:</b> 7 Year(s)<br/><b>Location:</b> New Jersey<br/><b>Industry Type:</b> Rx: Solid Dose / Tablets / Capsules<br/><b>Summary:</b> <div class="full_content"> <div class="main_content_box" id="description_box"> <div class="job_description"> <div class="job_qualifications"> <ul> <li> <div> <font face="Verdana" size="1">Experience managing direct reports (sourcing professional) with proven leadership results</font></div> </li> <li> <div> <font face="Verdana" size="1">Experience in Category Management strategy. Proven track record of supplier evaluation, negotiation and selection.</font></div> </li> <li> <div> <font face="Verdana" size="1">Experience in contract management and execution.</font></div> </li> <li> <div> <font face="Verdana" size="1">Experience in supplier development and supplier performance.</font></div> </li> <li> <div> <font face="Verdana" size="1">Strong skills in spend and performance analysis.</font></div> </li> <li> <div> <font face="Verdana" size="1">Good understanding of supply market</font></div> </li> <li> <div> <font face="Verdana" size="1">Good understanding of best-in-class sourcing management processes and techniques. Knowledge of ePurchasing tools (e.g. Ariba, SAP, JDE etc) would be an advantage</font></div> </li> <li> <div> <font face="Verdana" size="1">Ability to identify business opportunities and prepare business proposals.</font></div> </li> <li> <div> <font face="Verdana" size="1">Energetic, committed and dedicated to achieve success.</font></div> </li> <li> <div> <font face="Verdana" size="1">Able to resolve problem, transition and transform sourcing activities</font></div> </li> <li> <div> <font face="Verdana" size="1">Excellent interpersonal, communication and presentation skills.</font></div> </li> <li> <div> <font face="Verdana" size="1">Personal organization and self-management.</font></div> </li> </ul> <p style="MARGIN-BOTTOM: 0px; MARGIN-TOP: 0px"> <b><font color="#565656" face="Verdana" size="1">Minimum Requirements and Education:</font></b></p> <ul> <li> <div> <font face="Verdana" size="1">Experience in Pharmaceutical marketing preferred</font></div> </li> <li> <div> <font face="Verdana" size="1">Procurement related degree preferred.</font></div> </li> <li> <div> <font face="Verdana" size="1">&nbsp;7-10 years relevant management level experience in a procurement related environment desirable.</font></div> </li> </ul> </div> </div> </div> </div> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=777 http://pharmaboard.com/empid=777 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Sen. Manager, Regulatory Affairs <b>Experience:</b> 5 Year(s)<br/><b>Location:</b> California<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <div> <font color="black" face="Arial"><font size="2"><strong><em><font color="#565656">Requirements</font></em></strong> </font></font> <ul> <li> <div> <font color="black" face="Arial"><font size="2"><font face="Arial" size="2">Leadership/management experience preferred.</font></font></font></div> </li> <li> <div> <font color="black" face="Arial"><font size="2"><font face="Arial" size="2">Experience in an early stage company environment, preferably in medical devices or combination products.</font></font></font></div> </li> <li> <div> <font color="black" face="Arial"><font size="2"><font face="Arial" size="2">Knowledge of FDA, CA-FDB, and ISO regulations/standards, including ISO 10993 (requirements for biocompatibility).</font></font></font></div> </li> <li> <div> <font color="black" face="Arial"><font size="2"><font face="Arial" size="2">RAC certification in US, EU, and/or CAN is a plus.</font></font></font></div> </li> <li> <div> <font color="black" face="Arial"><font size="2"><font face="Arial" size="2">Working knowledge of project planning and management including use of PM software such as MS Project is a plus.</font></font></font></div> </li> <li> <div> <font color="black" face="Arial"><font size="2"><font face="Arial" size="2">Ability to focus on and achieve scheduled milestones, including contingency planning.</font></font></font></div> </li> <li> <div> <font color="black" face="Arial"><font size="2"><font face="Arial" size="2">Strong team-working and communication skills.&nbsp; A drive to get the job done in the face of obstacles and time constraints, and a willingness to jump in wherever needed.</font></font></font></div> </li> <li> <div> <font color="black" face="Arial"><font size="2"><font face="Arial" size="2">Competent using office software including MS Word, Excel, Internet Explorer, PowerPoint, and Outlook.</font></font></font></div> </li> <li> <div> <font color="black" face="Arial"><font size="2"><font color="black" face="Arial" size="2">Responsible for performing all duties in compliance with FDA&rsquo;s Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which ZELTIQ complies.<font color="black" face="Arial" size="1">&nbsp;&nbsp;</font></font></font></font></div> </li> </ul> </div> <div> <div> <b><i><font color="black" face="Arial"><font size="2">Education<font color="black" face="Arial">&nbsp;</font></font></font></i></b></div> </div> <ul> <li> <div> <font face="Arial" size="2">BS or BA degree plus seven years&rsquo; experience in regulatory affairs, and at least five years in medical devices.</font></div> </li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=776 http://pharmaboard.com/empid=776 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Associate Director, Products CMC Program Leader <b>Experience:</b> 7 Year(s)<br/><b>Location:</b> Connecticut<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <p> <strong>Qualifications</strong></p> <ul> <li> Minimum of 7 years&rsquo; of experience in the biopharmaceutical industry, with minimum of 3 years&nbsp;in a CMC Project/Program Management role, specific to devices and combination products</li> <li> Deep experience with the CMC development and regulatory pathway specifically associated with combination products and drug delivery devices</li> <li> Demonstrated ability to organize and lead teams</li> <li> Demonstrated tactical capabilities with forward looking perspective</li> <li> Strong communication, leadership and collaboration skills are required</li> <li> High level of proficiency in MS Office software including: Word, Excel, Outlook, Visio, Project and PowerPoint. Knowledge of MS Project Server a plus</li> <li> Strong interpersonal skills; fluent and able to influence others in spoken and written English</li> </ul> <p> <strong>Education </strong></p> <ul> <li> Bachelors&rsquo; degree in scientific discipline</li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=774 http://pharmaboard.com/empid=774 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Executive Director, Clinical Data Management <b>Experience:</b> 0 Year(s)<br/><b>Location:</b> Massachusetts<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <p> <strong>Essential Qualifications</strong></p> <ul> <li> Bachelors of Science degree required, Master in Science in health related field, preferred together with 15 years&rsquo; of pharmaceutical experience including ten (10) years&#39; of supervisory and management experience in the pharmaceutical research environment;</li> <li> Strong data management and EDC experience required including CDISC, 21 CFR Part 11,&nbsp; ICH/GCP guidelines, and clinical trial methodology. Medidata Rave experience is preferred;</li> <li> Strong project management skills and experience with scope management, resource management, financial management, project planning and resource allocation;</li> <li> Experience partnering and driving CRO relationships and other external resources;</li> <li> Experienced enterprise leader capable of integrating across functional boundaries;</li> <li> A detail-oriented team player with strong organizational skills and the ability to multi-task, prioritize and plan within a high-energy setting to build a solutions based environment;</li> <li> Excellent verbal and written communication skills, and excellent inter-personal skills;</li> <li> Flexible, well-organized, and able to lead well under pressure.</li> </ul> <p> <strong>Preferred Qualifications</strong></p> <ul> <li> Up-to-date with industry advancements around data standards and data related technologies including their implementation;</li> <li> Experience working in a clinical development organization with a heavy emphasis on support of multiple, ongoing projects.</li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=773 http://pharmaboard.com/empid=773 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Stability Associate I, Pharmaceutical Development <b>Experience:</b> 2 Year(s)<br/><b>Location:</b> Connecticut<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <p> <strong>Qualifications</strong></p> <ul> <li> A successful candidate will typically have +2 years&rsquo; of experience working in a relevant laboratory setting</li> <li> Knowledge of GMPs and their application in the environment is preferred.&nbsp;</li> <li> Have a strong working knowledge of governing documents for stability.</li> <li> Able to understand and follow written procedures.</li> <li> Document reported stability data in tables for reporting and trending with a strong attention to detail; able to recognize trends outside of expected results.</li> <li> Able to organize his/her own work on a routine basis and requires minimal supervision. When asked, the individual is able to provide updates and tracking on his/her tasks.</li> <li> The ability to communicate verbally and in a written format is required.</li> <li> Ability to interact with Analytical Sciences Operations groups, Quality Assurance and GPD members.</li> <li> Able to navigate external vendor sites and portals for data extraction and review.</li> <li> Able to communicate findings to colleagues within the group through presentations.</li> <li> Proficient with various MS Office programs, including Word, Excel, Outlook, FirstDocs and PowerPoint as well as SAS JMP statistical software.</li> </ul> <p style="margin-left:.25in;"> &nbsp;</p> <p> <strong>Education </strong></p> <ul> <li> A successful candidate will typically hold a BS degree in Biochemistry, Chemistry, Chemical Engineering or related discipline from an accredited university with 2-5 years&rsquo; of relevant experience or equivalent combination of education and experience.</li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=772 http://pharmaboard.com/empid=772 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Associate Director, Clinical Project Lead <b>Experience:</b> 10 Year(s)<br/><b>Location:</b> Massachusetts<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <p> <strong>Essential Qualifications</strong></p> <ul> <li> &gt;10 years&rsquo; of clinical research experience, 5 of which in a leading role accountable for the planning and execution of global clinical trials.</li> <li> Bachelor&rsquo;s degree or equivalent in one of the disciplines related to clinical practice/health care, life sciences, or drug development.</li> <li> Ability to lead cross-functional teams and to provide management oversight of CROs.</li> <li> Experience in developing study budgets, forecasting and financial oversight of a project.</li> </ul> <p style="margin-left:.25in;"> &nbsp;</p> <p> <strong>Preferred Qualifications</strong></p> <ul> <li> Advanced degree (Master, PhD, MD) is desirable.</li> <li> PMP certification desirable.</li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=771 http://pharmaboard.com/empid=771 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Director, Competitive Intelligence <b>Experience:</b> 5 Year(s)<br/><b>Location:</b> Massachusetts<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <p> <strong>Essential Qualifications</strong></p> <ul> <li> Advanced degree in a scientific field. &nbsp;</li> <li> Demonstrated excellence in scientific evaluation.</li> <li> Demonstrated business acumen.</li> <li> 5-8 years&rsquo; of R&amp;D/ commercial or BD experience within a related field or equivalent combination of education and biotech/pharma experience.</li> <li> Strong project management /tracking skills to monitor multiple assessments in short timeframe</li> <li> Excellent communication skills both written and verbal.</li> <li> Strong presentation skills to deliver recommendations and frame business case consideration to senior stakeholders internally and externally.</li> <li> Excellent interpersonal skills with demonstrated track record and ability to drive results as an effective a team member and project leader.</li> <li> Must demonstrate an energy and enthusiasm which brings a positive approach to all challenges.</li> <li> Sense of ethics and responsibility.</li> <li> Ability to travel as required to meet business needs.</li> </ul> <p> <strong>Preferred Qualifications </strong></p> <ul> <li> Experience in competitive intelligence function or similar commercial/ business development function at a biotech or pharma organization</li> <li> Strong collaboration, relationship building / networking skills.</li> <li> Excellent problem solving skills.</li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=770 http://pharmaboard.com/empid=770 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Sen. Dir. Global Ops Quality Compliance <b>Experience:</b> 15 Year(s)<br/><b>Location:</b> Connecticut<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <p style="margin-left:36.0pt;"> &nbsp;</p> <p> <a href="http://jobs.alexion.com/job/7973492/senior-director-global-operations-quality-compliance-new-haven-ct/#PrincipalResponsibilities"><strong>Essential Qualifications</strong></a></p> <ul> <li> Minium 15 years experience in GMP Quality/Compliance environment and 5 years in a relevant managerial role</li> <li> Experience leading and managing across a matrix with strong influence management experience and ability to manage a team of experts</li> <li> Thorough knowledge of applicable international GxP regulations and standards</li> <li> Ability to provide technical and compliance related direction</li> <li> Ability to coordinate efforts across multiple functions to maintain optimal performance.</li> <li> Sound pharmaceutical industry awareness and understanding, especially with respect to quality and regulatory requirements</li> <li> Strong mature leader with influencing skills</li> <li> Ability to represent the company both internally and externally</li> </ul> <ul> <li> Strong verbal and written communication skills with ability to present to various audience levels</li> <li> Strong ability to analyze systems, data</li> <li> Capable of identifying and mitigating risks</li> </ul> <p> &nbsp;</p> <p> <strong>Preferred Qualifications </strong></p> <ul> <li> BS/BA in science or related field. MS preferred</li> </ul> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=769 http://pharmaboard.com/empid=769 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Associate Medical Director, U.S. Medical Affairs <b>Experience:</b> 4 Year(s)<br/><b>Location:</b> Massachusetts<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <p> <strong>Essential Qualifications</strong></p> <ul> <li> Minimum 4 years&rsquo; of relevant experience</li> <li> Medical degree (M.D.), Pharm D or Ph D</li> <li> Demonstrated ability to create and lead successful cross-functional teams in changing, competitive environments</li> <li> Good analytical skills as applied to medical, scientific and technical information.</li> <li> Demonstrated ability to accurately and effectively evaluate medical/scientific literature and develop effective medical strategies and communication strategies.</li> <li> Excellent written and verbal communication skills in both local language and in English</li> <li> Adaptability to multicultural environment</li> <li> Ethics and values with Integrity and Trust</li> </ul> <p> &nbsp;</p> <p> <strong>Preferred Qualifications </strong></p> <ul> <li> 2+ years&rsquo; in medical affairs</li> <li> Product lifecycle management experience</li> <li> Orphan diseases knowledge/experience</li> <li> Demonstrated ability to influence important customers, challenge common perceptions and implement medical affairs tools to improve patient care and outcomes</li> <li> Demonstrated experience in early and late clinical development.</li> <li> Strategic agility</li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=768 http://pharmaboard.com/empid=768 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Sen. Manager, Tech-Ops - Transgenic <b>Experience:</b> 10 Year(s)<br/><b>Location:</b> Massachusetts<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <p> <strong>Qualifications</strong></p> <ul> <li> Minimum of 8 years&rsquo; of relevant experience in a commercial biopharmaceutical manufacturing environment is required.</li> <li> Strong quality mindset and willingness to take ownership of challenges.</li> <li> Ability to document, present and defend technical and scientific approaches and decisions in both written and verbal form to internal and external partners.&nbsp;</li> <li> &nbsp;&nbsp;Act as an SME for both major and critical deviations and support regulatory inspections as required.</li> <li> &nbsp;&nbsp;Must be able to assemble and coordinate the activities of cross functional teams.&nbsp;</li> <li> Self-starter that can carry out tasks with minimal oversight.</li> <li> &nbsp;&nbsp;Experience with aseptic &nbsp;&nbsp;technique is preferred.</li> <li> 20% travel</li> </ul> <p> <strong>Education </strong></p> <ul> <li> BS or MS in Engineering or Scientific discipline.</li> <li> BS with 10 years&rsquo; of relevant experience, or MS with 7 years&rsquo; of relevant experience. &nbsp;PHD with 2 years&rsquo; of relevant experience.</li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=767 http://pharmaboard.com/empid=767 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Director, Global Regulatory Affairs Opex <b>Experience:</b> 5 Year(s)<br/><b>Location:</b> Massachusetts<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <p> <strong>Qualifications</strong></p> <ul> <li> Experience in the pharmaceutical industry with &nbsp;&nbsp;min 5 years regulatory affairs experience</li> <li> Strong communications skills: oral, written, with proven negotiation skills, and strong time-management</li> <li> Must have the ability to work within a global team framework and maintain a global perspective;</li> <li> Project Management skills&nbsp;</li> <li> Ability to lead and respond to changing environment</li> <li> A critical logical thinker with the ability to analyze problems, identify alternative solutions and implement recommendations for resolution</li> <li> Demonstrated experience in project management The ability to multitask and manage multiple changing priorities</li> <li> General medical knowledge</li> <li> Proven ability to work under pressure and adhere to deadlines</li> <li> Strong analytical skills and ability to interpret data and make strategic decisions around regulatory strategy</li> <li> Must have the ability to work within a global team framework and maintain a global perspective;</li> <li> Demonstrated high performance orientation, detail orientation, organization skills, and market knowledge;</li> <li> Excellent written, listening, and verbal communication skills as well as analytical skills;</li> <li> Demonstrated strong influencing skills and consensus building skills.</li> </ul> <p> &nbsp;</p> <p> <strong>Education </strong></p> <ul> <li> Degree in bio-pharma-related area</li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=766 http://pharmaboard.com/empid=766 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com cGMP Lead Associate, 2nd shift <b>Experience:</b> 1 Year(s)<br/><b>Location:</b> New Jersey<br/><b>Industry Type:</b> Rx: Sterile aseptic<br/><b>Summary:</b> <p> <strong><font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">EDUCATION AND EXPERIENCE:</font></font></strong><br /> &nbsp;<br /> &nbsp;</p> <ul dir="ltr"> <li> <font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">3-5 years minimum pharmaceutical experience</font></font></li> <li> <font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">Experience in a cGMP environment</font></font></li> <li> <font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">Experience in aseptic processing including formulation filling and packaging</font></font></li> <li> <font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">Experience in aseptic gowning </font></font></li> <li> <font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">Excellent oral and written communication skills</font></font></li> </ul> <p> &nbsp;<br /> <strong><font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">JOB PREREQUISITES:</font></font></strong><br /> &nbsp;<br /> &nbsp;</p> <ul dir="ltr"> <li> <font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">Ability to meet attendance standards.&nbsp; All full-time employees are required to work a 40 hour week, most of which has to be during &ldquo;regular&rdquo; business hours. At times it may be necessary to work additional hours in order to get the required tasks accomplished to meet deadlines.</font></font></li> <li> <font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">Hands on experience required to manage and trouble shoot major projects. </font></font></li> </ul> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=765 http://pharmaboard.com/empid=765 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Supervisor, Quality Assurance Documentation <b>Experience:</b> 2 Year(s)<br/><b>Location:</b> New Jersey<br/><b>Industry Type:</b> Rx: Sterile aseptic<br/><b>Summary:</b> <p> <strong><font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">QUALIFICATIONS:</font></font></strong><br /> <font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</font></font><br /> &nbsp;<br /> <strong><font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">EDUCATION AND EXPERIENCE:</font></font></strong><br /> &nbsp;<br /> <font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">Bachelor&rsquo;s degree (BS) from four year college or university: plus at least two (2) years&rsquo; experience in the pharmaceutical industry, in a documentation processing or related discipline.&nbsp; </font></font><br /> &nbsp;<br /> <strong><font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">JOB PREREQUISITES:</font></font></strong><br /> &nbsp;<br /> &nbsp;</p> <ul dir="ltr"> <li style="TEXT-ALIGN: justify"> <font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">Ability to meet attendance standards.&nbsp; All full-time employees are required to work a 40-hr week.&nbsp; At times it may be necessary to work additional hours in order to get the required tasks accomplished to meet deadlines. </font></font></li> <li style="TEXT-ALIGN: justify"> <font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">Must be detail oriented. </font></font></li> <li style="TEXT-ALIGN: justify"> <font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">Must have accomplished skills in computer-assisted documentation systems.</font></font></li> <li style="TEXT-ALIGN: justify"> <font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">Must have GMP experience in an FDA related environment, inclusive of 21 CFR Part 11 compliance criteria. </font></font></li> <li style="TEXT-ALIGN: justify"> <font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">Must have a team work attitude. </font></font></li> <li style="TEXT-ALIGN: justify"> <font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">Will interact with all functional departments within the company including hourly, professional and management personnel. </font></font></li> </ul> <p> &nbsp;<br /> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=764 http://pharmaboard.com/empid=764 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com QA Auditor 10:30 AM to 6:00 PM Shift <b>Experience:</b> 1 Year(s)<br/><b>Location:</b> Illinois<br/><b>Industry Type:</b> Rx: Sterile aseptic<br/><b>Summary:</b> <p> QUALIFICATIONS<br /> To perform this job successfully, an individual must be detail-oriented and possess the ability to multi-task and work on multiple projects simultaneously.&nbsp; &nbsp;An individual must be able to perform each essential duty satisfactorily.&nbsp; The requirements listed are representative of the knowledge, skill, and/or ability required.&nbsp; Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.<br /> &nbsp;<br /> SAFETY REQUIREMENTS<br /> Safety glasses, close-toed shoes and latex gloves are required in many areas within the facility<br /> &nbsp;<br /> &nbsp;<br /> EDUCATION AND EXPERIENCE<br /> High school diploma or GED required.<br /> One year of quality manufacturing experience preferred.&nbsp;&nbsp;</p> <p> JOB PREREQUISITES<br /> All full-time employees are required to work a 40 hour week.&nbsp; At times, additional hours during the weekdays, evenings and/or weekends will be required to complete tasks and meet deadlines.&nbsp; All applicants must be able to meet the attendance standards.&nbsp;<br /> Must have a complete knowledge of current Good Manufacturing Practices, United States Pharmacopea, current Code of Federal Regulations (21 CFR parts 11, 210, 211, 820) and other FDA regulations and guidance&rsquo;s.&nbsp;<br /> Have general math skills; adding, subtracting, multiplication, division and percentage calculation.&nbsp; Ability to calculate figures and amounts such as discounts, interest, commissions, and proportions.<br /> Able to use personal computer and standard office equipment such as fax and copy machines, calculator, and printers.&nbsp; Aptitude to learn computer programs as needed (i.e. Word, Excel) in addition to other business applications.<br /> Strong verbal and written communication skills.&nbsp; Resourceful and well organized.<br /> <br /> Ability to read and interpret standard documents such as:&nbsp; procedure manuals, employee handbook, job related publications. Ability to write routine reports and correspondence.<br /> <br /> Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.&nbsp; Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.&nbsp;</p> <p> PHYSICAL DEMANDS/ MENTAL DEMANDS AND WORK ENVIRONMENT<br /> While performing the duties of this job, the employee is regularly required to sit, stand, walk, talk and hear.&nbsp; The employee is required to use hands to finger, handle, or feel. May require the ability to lift up to 50 pounds.&nbsp; Specific vision abilities required by this job include close vision for written work, PC use and evaluation of test specimens.<br /> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=763 http://pharmaboard.com/empid=763 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com QA Data Reviewer <b>Experience:</b> 3 Year(s)<br/><b>Location:</b> Illinois<br/><b>Industry Type:</b> Rx: Sterile aseptic<br/><b>Summary:</b> <p> <strong>QUALIFICATIONS</strong><br /> To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.<br /> &nbsp;<br /> <strong>EDUCATION AND EXPERIENCE</strong><br /> Bachelor&rsquo;s degree (BS) in the Life Sciences (e.g., Chemistry, Biochemistry, or closely related field) or Pharmacy from an accredited four-year college or university<br /> 3 or more years of demonstrated excellence in an industrial laboratory related to pharmaceutical manufacturing, specializing in sterile dosage forms.&nbsp;<br /> <strong>JOB PREREQUISITES</strong><br /> Ability to meet attendance standards.&nbsp; All full-time employees are required to work a 40-hr week.&nbsp; At times it may be necessary to work additional hours in order to get the required tasks accomplished to meet deadlines.<br /> Must have complete knowledge of current Good Manufacturing Practices, United States Pharmacopea, Current Federal Register (CFR) and other applicable FDA regulations or guidelines.&nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=762 http://pharmaboard.com/empid=762 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Supervisor, Quality In-Process Audits - 2nd shift <b>Experience:</b> 5 Year(s)<br/><b>Location:</b> Illinois<br/><b>Industry Type:</b> Rx: Sterile aseptic<br/><b>Summary:</b> <div class="ng-scope" ng-class="jobDetailFields.isSocialReferralJobRestricted ? 'restrictedJobApplyMargin':''" ng-repeat="oQ in jobDetailFields.JobDetailQuestions | showJobDetailsFields track by $index"> <p class="answer ng-scope section2LeftfieldsInJobDetails jobDetailTextArea" j-query="html(oQ.AnswerValue)" ng-class="oQ.ClassName" ng-if="oQ.ClassName != 'jobtitleInJobDetails' &amp;&amp; oQ.ClassName != 'jobdescriptionInJobDetails'"> EDUCATION AND EXPERIENCE<br /> &bull;&nbsp;&nbsp; &nbsp;Bachelor&rsquo;s Degree (BS or BA) from a 4 year college or university<br /> &bull;&nbsp;&nbsp; &nbsp;5+ years demonstrated excellence in in the pharmaceutical or related industry<br /> <br /> JOB PREREQUISITES<br /> &bull;&nbsp;&nbsp; &nbsp;All full-time employees are required to work a 40 hour week. &nbsp;At times, additional hours during the weekdays, evenings and/or weekends will be required to complete tasks and meet deadlines. &nbsp;All applicants must be able to meet the attendance standards. &nbsp;<br /> &bull;&nbsp;&nbsp; &nbsp;Must have a complete knowledge of current Good Manufacturing Practices, United States Pharmacopea, current Code of Federal Regulations (21 CFR parts 11, 210, 211, 820) and other FDA regulations and guidance&rsquo;s. &nbsp;<br /> &bull;&nbsp;&nbsp; &nbsp;Strong verbal and written communication skills. &nbsp;Resourceful and well organized.&nbsp;<br /> &bull;&nbsp;&nbsp; &nbsp;Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. &nbsp;Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.<br /> &nbsp;</p> </div> <div class="ng-scope" ng-class="jobDetailFields.isSocialReferralJobRestricted ? 'restrictedJobApplyMargin':''" ng-repeat="oQ in jobDetailFields.JobDetailQuestions | showJobDetailsFields track by $index"> <p class="question thick ng-scope ng-binding section2LeftfieldsInJobDetails jobDetailTextArea" ng-bind-html="$root.utils.htmlEncode(oQ.QuestionName)" ng-class="oQ.ClassName" ng-if="oQ.QuestionName != ''"> &nbsp;</p> </div> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=761 http://pharmaboard.com/empid=761 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Production Supervisor, Packaging <b>Experience:</b> 3 Year(s)<br/><b>Location:</b> New Jersey<br/><b>Industry Type:</b> Rx: Sterile non-aseptic<br/><b>Summary:</b> <p> <strong><font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">QUALIFICATIONS:</font></font></strong><br /> <font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.&nbsp; The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. </font></font><br /> &nbsp;<br /> <strong><font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">EDUCATION AND EXPERIENCE:</font></font></strong><br /> &nbsp;<br /> <font style="FONT-FAMILY: garamond, serif; size: undefined"><font style="FONT-SIZE: 12pt">Associate&rsquo;s degree and/or 5 years experience as a supervisor, preferably in a pharmaceutical packaging environment.</font></font><br /> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=760 http://pharmaboard.com/empid=760 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com QA Line Monitor <b>Experience:</b> 1 Year(s)<br/><b>Location:</b> New York<br/><b>Industry Type:</b> Rx: Sterile non-aseptic<br/><b>Summary:</b> <p> <strong><font style="color:undefined;font-family:garamond,serif;size:undefined;"><font style="font-size:12.0pt;">QUALIFICATIONS</font></font></strong><br /> <br /> <font style="color:undefined;font-family:garamond,serif;size:undefined;"><font style="font-size:12.0pt;">To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.&nbsp; The requirements listed are representative of the knowledge, skill, and/or ability required.&nbsp;&nbsp;&nbsp; Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</font></font><br /> &nbsp;</p> <ul dir="ltr"> <li> <font style="color:undefined;font-family:garamond,serif;size:undefined;"><font style="font-size:12.0pt;">Good communication skills (written and verbal)</font></font></li> <li> <font style="color:undefined;font-family:garamond,serif;size:undefined;"><font style="font-size:12.0pt;">Ability to work well with people and independently</font></font></li> <li> <font style="color:undefined;font-family:garamond,serif;size:undefined;"><font style="font-size:12.0pt;">Experience in a Quality environment</font></font></li> <li> <font style="color:undefined;font-family:garamond,serif;size:undefined;"><font style="font-size:12.0pt;">Must have knowledge of cGMPs and SOPs</font></font></li> <li> <font style="color:undefined;font-family:garamond,serif;size:undefined;"><font style="font-size:12.0pt;">Must be able to follow written and verbal instructions and ability to read and understand SOPs. </font></font></li> <li> <font style="color:undefined;font-family:garamond,serif;size:undefined;"><font style="font-size:12.0pt;">Must possess excellent time management skills </font></font></li> <li> <font style="color:undefined;font-family:garamond,serif;size:undefined;"><font style="font-size:12.0pt;">Good organizational skills</font></font></li> <li> <font style="color:undefined;font-family:garamond,serif;size:undefined;"><font style="font-size:12.0pt;">Basic mathematical skills</font></font></li> <li> <font style="color:undefined;font-family:garamond,serif;size:undefined;"><font style="font-size:12.0pt;">Attention to detail is critical</font></font></li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=759 http://pharmaboard.com/empid=759 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Sr. Manager, Aseptic Technical Engineering <b>Experience:</b> 10 Year(s)<br/><b>Location:</b> Illinois<br/><b>Industry Type:</b> Rx: Sterile aseptic<br/><b>Summary:</b> <p class="question thick ng-scope ng-binding section2LeftfieldsInJobDetails jobDetailTextArea" ng-bind-html="$root.utils.htmlEncode(oQ.QuestionName)" ng-class="oQ.ClassName" ng-if="oQ.QuestionName != ''"> Qualifications</p> <p class="answer ng-scope section2LeftfieldsInJobDetails jobDetailTextArea" j-query="html(oQ.AnswerValue)" ng-class="oQ.ClassName" ng-if="oQ.ClassName != 'jobtitleInJobDetails' &amp;&amp; oQ.ClassName != 'jobdescriptionInJobDetails'"> &nbsp;</p> <div dir="ltr" style="margin-top:5.0pt;margin-right:0in;margin-bottom:0in;margin-bottom:.0001pt;text-align:justify;"> <ul> <li> Bachelor of Science (BS) in Chemical or Mechanical Engineering from an accredited college.</li> <li> The individual must have a minimum of 10-years of experience in the traditional clean room aseptic pharmaceutical industry.</li> <li> The individual must have a minimum of 5 years of experience in a managerial role.</li> <li> Experience with Validation Lifecyle Documentation is required.</li> <li> Experience with the design, specification, and troubleshooting of facility, critical utility, and aseptic process equipment is required.</li> <li> Aseptic process equipment maintenance experience is required.</li> <li> CMMS/CCMS experience is required.</li> <li> Automation system experience (SCADA, MES, BAS) is required.</li> <li> Experience with RABs is preferred.</li> <li> Technical training in aseptic building design is preferred.</li> <li> Packaging equipment experience is beneficial.</li> <li> Excellent communications skills in oral, written, and presentation situations providing clear, informative, and persuasive communication in positive and negative scenarios.</li> <li> Good analytical and computer skills required.</li> </ul> </div> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=758 http://pharmaboard.com/empid=758 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Quality Assurance Supervisor, 2nd shift <b>Experience:</b> 5 Year(s)<br/><b>Location:</b> New Jersey<br/><b>Industry Type:</b> Rx: Sterile aseptic<br/><b>Summary:</b> <p> <span style="COLOR: #333333"><font style="FONT-FAMILY: verdana, sans-serif; size: undefined"><font style="FONT-SIZE: 8.5pt"><strong>QUALIFICATIONS</strong><br /> To perform this job successfully, an individual must be detail-oriented and possess the ability to multi-task and work on multiple projects simultaneously. &nbsp; An individual must be able to perform each essential duty satisfactorily. &nbsp;The requirements listed are representative of the knowledge, skill, and/or ability required. &nbsp;Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.<br /> <br /> <strong>SAFETY REQUIREMENTS</strong><br /> Safety glasses, close-toed shoes and latex gloves are required in many areas within the facility&nbsp;<br /> <br /> <strong>EDUCATION AND EXPERIENCE</strong><br /> &bull;&nbsp;&nbsp; &nbsp;Bachelor&rsquo;s Degree (BS or BA)&nbsp;<br /> &bull;&nbsp;&nbsp; &nbsp;5-10 years demonstrated excellence in in the pharmaceutical or related industry<br /> <br /> <strong>JOB PREREQUISITES</strong><br /> &bull;&nbsp;&nbsp; &nbsp;All full-time employees are required to work a 40 hour week. &nbsp;At times, additional hours during the weekdays, evenings and/or weekends will be required to complete tasks and meet deadlines. &nbsp;All applicants must be able to meet the attendance standards. &nbsp;<br /> &bull;&nbsp;&nbsp; &nbsp;Must have a complete knowledge of current Good Manufacturing Practices, United States Pharmacopea, current Code of Federal Regulations (21 CFR parts 11, 210, 211, 820) and other FDA regulations and guidance&rsquo;s. &nbsp;<br /> &bull;&nbsp;&nbsp; &nbsp;Have general math skills; adding, subtracting, multiplication, division and percentage calculation. &nbsp;Ability to calculate figures and amounts such as discounts, interest, commissions, and proportions.<br /> &bull;&nbsp;&nbsp; &nbsp;Able to use personal computer and standard office equipment such as fax and copy machines, calculator, and printers. &nbsp;Aptitude to learn computer programs as needed (i.e. Word, Excel) in addition to other business applications.<br /> &bull;&nbsp;&nbsp; &nbsp;Strong verbal and written communication skills. &nbsp;Resourceful and well organized.&nbsp;<br /> o&nbsp;&nbsp; &nbsp;Ability to read and interpret standard documents such as: &nbsp;procedure manuals, employee handbook, job related publications. Ability to write routine reports and correspondence.<br /> &bull;&nbsp;&nbsp; &nbsp;Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. &nbsp;Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.</font></font></span></p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=757 http://pharmaboard.com/empid=757 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Packaging Engineer <b>Experience:</b> 3 Year(s)<br/><b>Location:</b> New York<br/><b>Industry Type:</b> Rx: Liquids / Topicals / Powders / Softgel<br/><b>Summary:</b> <p class="question thick ng-scope ng-binding section2LeftfieldsInJobDetails jobDetailTextArea" ng-bind-html="$root.utils.htmlEncode(oQ.QuestionName)" ng-class="oQ.ClassName" ng-if="oQ.QuestionName != ''"> Qualifications</p> <p class="answer ng-scope section2LeftfieldsInJobDetails jobDetailTextArea" j-query="html(oQ.AnswerValue)" ng-class="oQ.ClassName" ng-if="oQ.ClassName != 'jobtitleInJobDetails' &amp;&amp; oQ.ClassName != 'jobdescriptionInJobDetails'"> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</font></p> <ol dir="ltr"> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Thorough understanding of packaging performance test methods (compression testing, drop testing, vibration testing).</font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Understanding of the impact of packaging on manufacturing, material handling, and logistics/distribution.</font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Demonstrated knowledge of various packaging types, materials (foils, laminates, polymers) and manufacturing technologies such as thermos-forming &amp; form/fill/seal. </font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Strong project management skills. </font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Able to excel in a cross-functional working environment.</font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Ability to multi-task, prioritize and handle multiple projects at once.</font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Excellent interpersonal communications with variety of departments with varying objectives.</font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Must have strong communication and writing skills in English.</font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Must have a solid understanding of packaging materials, capabilities, and equipment </font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Needs to be able to collaborate with other teams, as well as maintain and strengthen cross departmental relationships.</font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Must have strong analytical and logical problem solving abilities.</font></li> </ol> <p> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">&nbsp;<br /> <strong>Education and Experience</strong></font></p> <ol dir="ltr"> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">BS in Package Engineering with a minimum of 3-5 years of experience in the pharmaceutical or related industry.</font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Strong project management and organizational skills, prioritizes and plans work activities; uses time efficiently; plans for additional resources; sets goals and objectives; organizes or schedules other people and their tasks; develops realistic action plans.</font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Follows instructions, responds to management direction; takes responsibility for own actions; keeps commitments; commits to long hours of work when necessary to reach goals; completes tasks on time or notifies appropriate person with an alternate plan.</font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Demonstrates accuracy and thoroughness; looks for ways to improve and promote quality; applies feedback to improve performance; monitors own work to ensure high quality.</font></li> </ol> <p> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">&nbsp;<br /> <strong>Job Prerequisites</strong></font></p> <ol dir="ltr"> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Demonstrated skills in collaborating and influencing cross-functional groups including strong interpersonal skills. </font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Hands on experience required to troubleshoot projects. </font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Knowledge of US FDA and International cGMP guidelines.</font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">A working knowledge of pharmaceutical product development and US FDA filing requirements for packaging.</font></li> </ol> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=756 http://pharmaboard.com/empid=756 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Supervisor, Method Transfers/Verifications <b>Experience:</b> 0 Year(s)<br/><b>Location:</b> New Jersey<br/><b>Industry Type:</b> Rx: Sterile non-aseptic<br/><b>Summary:</b> <p class="question thick ng-scope ng-binding section2LeftfieldsInJobDetails jobDetailTextArea" ng-bind-html="$root.utils.htmlEncode(oQ.QuestionName)" ng-class="oQ.ClassName" ng-if="oQ.QuestionName != ''"> Qualifications</p> <p class="answer ng-scope section2LeftfieldsInJobDetails jobDetailTextArea" j-query="html(oQ.AnswerValue)" ng-class="oQ.ClassName" ng-if="oQ.ClassName != 'jobtitleInJobDetails' &amp;&amp; oQ.ClassName != 'jobdescriptionInJobDetails'"> &nbsp;</p> <ul dir="ltr"> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Bachelor&rsquo;s Degree (BS or BA) or M.S. in Chemistry</font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Minimum of 5-years experience in analytical method development</font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Strong working knowledge of HPLC, UPLC, GC and ICP-MS</font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Experience working in a GMP laboratory setting</font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Good oral and verbal communication skills</font></li> <li> <font style="color:undefined;font-family:arial,helvetica,sans-serif;size:undefined;">Proactive and has good problem solving skills</font></li> </ul> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=755 http://pharmaboard.com/empid=755 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Senior Quality Analyst (QA) <b>Experience:</b> 2 Year(s)<br/><b>Location:</b> Puerto Rico<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <div align="left"> <font size="2">Qualifications:</font></div> <div align="left"> &nbsp;</div> <div align="left"> <font size="2">Basic:</font></div> <ul> <li> <div align="left"> <font size="2">Bachelor&#39;s degree in Biotechnology, Biology, Chemistry or Engineering.</font></div> </li> <li> <div align="left"> <font size="2">Master&#39;s degree: not required but desired.</font></div> </li> </ul> <p align="left" style="MARGIN-BOTTOM: 0px; MARGIN-TOP: 0px"> <font size="2">Technical Skills:</font></p> <p align="left" style="MARGIN-BOTTOM: 0px; MARGIN-TOP: 0px"> &nbsp;</p> <ul> <li> <div align="left"> <font size="2">Highly developed verbal and written communication skills in both Spanish and English.</font></div> </li> <li> <div align="left"> <font size="2">Highly developed problem solving and analytical skills.</font></div> </li> <li> <div align="left"> <font size="2">Highly developed interpersonal relations / communications skills.</font></div> </li> <li> <div align="left"> <font size="2">Highly developed negotiation skills.</font></div> </li> </ul> <div align="left"> &nbsp;</div> <div align="left"> <font size="2">Experience Required:</font></div> <div align="left"> &nbsp;</div> <ul> <li> <div align="left"> <font size="2">This position requires a professional with a broad spectrum of quality /compliance management skills. This position also requires knowledge of regulations and standards affecting APIs and</font> <font size="2">Biologics.</font></div> </li> <li> <div align="left"> <font size="2">Expertise in Quality Assurance, or Manufacturing, or Validation &ndash; 2 years.</font></div> </li> <li> <div align="left"> <font size="2">Experience in Health care industry &ndash; 6 years.</font></div> </li> <li> <div align="left"> <font size="2">Total combined minimum years of experience required</font></div> </li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=754 http://pharmaboard.com/empid=754 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Associate Scientific Compliance Specialist <b>Experience:</b> 3 Year(s)<br/><b>Location:</b> Illinois<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <div> <strong>Qualifications:</strong></div> <div> &nbsp;</div> <div> <strong>Basic Requirements for Position:</strong></div> <ul> <li> <div> BS degree and 3 years&rsquo; experience or MS degree in a scientific discipline, or equivalent experience.</div> </li> <li> <div> Ability to facilitate discussions and/or meetings while working in a matrixed environment.</div> </li> <li> <div> Good oral, written, interpersonal, and presentation skills.</div> </li> <li> <div> Knowledge and experience working within GxP regulations</div> </li> <li> <div> Working knowledge of regulations, processes, procedures, and documentation requirements for scientific studies and publications</div> </li> </ul> <div> &nbsp;&nbsp;</div> <div> <strong>Key Competencies:</strong></div> <ul> <li> <div> Builds strong working relationships with team members and cross-functional partners.</div> </li> <li> <div> Creates a learning environment, open to suggestions and experimentation for improvement.</div> </li> <li> <div> Embraces the ideas of others, nurtures innovation, and manages innovation to reality.</div> </li> <li> <div> Learns fast, grasps the &quot;essence&quot; and can change course quickly where indicated.</div> </li> <li> <div> Raises the bar and is never satisfied with the status quo.</div> </li> </ul> <p> &nbsp;</p> <p> <strong>Equal Opportunity Employer Minorities/Women/Veterans/Disabled</strong></p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=753 http://pharmaboard.com/empid=753 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Director, Biologics CMC Sciences <b>Experience:</b> 10 Year(s)<br/><b>Location:</b> Massachusetts<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <div> <div id="description_box"> <div> <div> <strong>Responsibilities Include:&nbsp;</strong></div> <div> <ul> <li> Lead biologics DS CMC Program leaders by providing clear direction as to their roles and responsibilities.</li> <li> Manage a coordinated approach across ABC, ABR, ABL and ABS biologics sites.</li> <li> Establish CMC strategy for DS development for all R&amp;D projects that is closely aligned with clinical/regulatory/development strategy.</li> <li> Establish CMC strategy for all approved biologics projects that is closely aligned with technical/manufacturing/regulatory/supply chain strategy and fulfills AbbVies business objectives.</li> <li> Participate in meeting with regulatory authorities and respond urgently to queries; support pre-approval inspections.</li> <li> Participate in management of partnered projects (alliance management) and active due diligence for potential in-licensing and acquisitions.</li> <li> Communicate R&amp;D demands to manufacturing and integrate into plan; develop costs/budgets for GPRD portfolio review.</li> <li> Management of direct reports and management of multi-functional CMC/program teams.</li> <li> Provide on-going CMC program management for R&amp;D and commercial biologics DS programs at each of the biologics plants/development sites worldwide.&nbsp;&nbsp;</li> </ul> </div> <div> <div> <strong>Qualifications:&nbsp;</strong></div> <div> <ul> <li> Ph.D. and 10+ years of experience [or equivalant] required with background in chemical engineering, biology,cell or molecular biology, biochemistry or other similar.</li> <li> Experience in biologics and two or more of the following areas: biologics development, biologics technical support/manufacturing experience, biotech industry, project or program management, managerial (including middle management), licensing or biologics business development, financial/budget responsibility&nbsp;</li> </ul> <strong>Equal Opportunity Employer Minorities/Women/Veterans/Disabled</strong></div> <div> <p> &nbsp;</p> <p> &nbsp;</p> <p> &nbsp;</p> <p> &nbsp;</p> </div> </div> </div> </div> </div> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=752 http://pharmaboard.com/empid=752 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Senior Manager, CMC Operations <b>Experience:</b> 14 Year(s)<br/><b>Location:</b> Massachusetts<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <div> <div id="description_box"> <div> <div> <strong>Qualifications Include:&nbsp;</strong> <ul> <li> Bachelor&rsquo;s Degree in Science related field with 16 years of related work [OR] Master&rsquo;s Degree Science/ PharmD with 14 years of related work [OR] PhD in Science or related field with 8+ years of related work experience.</li> <li> Project Management Professional (PMP) and/or APICS certification desired but not required</li> <li> Effective in influencing and negotiating with executive leadership; actively challenges project teams, drives to timely outcomes</li> <li> </li> <li> Proficient in project management tools</li> <li> Exceptional business acumen including project accounting and cost accounting; understands&nbsp;financial process and how to navigate to ensure accuracy and agility given changing priorities</li> </ul> <div> <strong>Equal Opportunity Employer Minorities/Women/Veterans/Disabled</strong></div> </div> </div> </div> </div> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=751 http://pharmaboard.com/empid=751 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Senior District Manager- Women\\\'s Health <b>Experience:</b> 5 Year(s)<br/><b>Location:</b> California<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <div class="full_content"> <div class="main_content_box" id="description_box"> <div class="job_description"> <div class="job_qualifications"> <ul> <li> <font size="2">rformance.</font></li> <li> <font size="2">Excellent judgment and decision making skills.</font></li> <li> <font size="2">Ability to articulate the scientific aspects of treatments and therapeutic area.</font></li> <li> <font size="2">Proven ability to deliver candid, effective feedback and efficiently manage performance.</font></li> <li> <font size="2">&nbsp;Ability to develop talent for promotional opportunities.</font></li> <li> <font size="2">Ability to create a culture of winning and full team engagement.</font></li> <li> <font size="2">Collaborates and is able to influence without authority across organizations.</font></li> <li> <font size="2">Models AbbVie&rsquo;s Ways of Working.</font></li> <li> <font size="2">2-3 years selling experience within the pharmaceutical industry or equivalent.</font></li> </ul> <p style="MARGIN-BOTTOM: 0px; MARGIN-TOP: 0px"> <font size="2">Preferred:</font></p> <ul> <li> <font size="2">1 to 2 years people management experience including coaching and development. </font></li> <li> <font size="2">Formal in house development role in training, marketing or other areas preferred.</font></li> <li> <font size="2">Women&rsquo;s Health experience preferred.</font></li> <li> <font size="2">Launch experience preferred.</font></li> </ul> <div> <p style="MARGIN-BOTTOM: 0px; MARGIN-TOP: 0px"> <font size="2"><strong><font size="2">Equal Opportunity Employer Minorities/Women/Veterans/Disabled&nbsp;</font></strong></font></p> </div> <p style="MARGIN-BOTTOM: 0px; MARGIN-TOP: 0px"> <font size="2">&nbsp;</font></p> </div> </div> </div> </div> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=750 http://pharmaboard.com/empid=750 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Global Marketing Director, Rheumatology <b>Experience:</b> 8 Year(s)<br/><b>Location:</b> Illinois<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <p> <strong><u>Key Skills:</u></strong></p> <ul> <li> Demonstrate high proficiency of the whole and the component parts of the Marketing skills framework: Insights, Segmentation, Positioning, Value Proposition, Business Model Innovation, Creative Development, Investment Optimization</li> <li> Grow and leverage team members&rsquo; Marketing skills</li> <li> Exhibit P&amp;L mindset regardless of role and/or unit</li> <li> Leverage data, analytics and strategic mind-set in all aspects of running the marketing component of the business</li> <li> Provide positive leadership and productive influence across and around the enterprise</li> <li> Effectively orchestrate work across internal teams and external partners including agencies, etc.</li> </ul> <p> <strong><u>Key Experiences/Assignments/Projects:</u></strong></p> <ul> <li> Foundational marketing experiences, including product management</li> <li> Cross-business experiences, including a portfolio of multiple franchise exposure: growth, mature and launch brands</li> <li> Cross-functional and/or similar experiences including field sales, finance, regulatory, research &amp; development and other relevant business functions, like Managed Care, Market Analytics and Business Insights.</li> <li> Cross-geography, including global and/or international experience</li> <li> Strategic initiatives</li> </ul> <div> <p> <strong><u>Qualifications:</u></strong></p> <ul> <li> Bachelor&rsquo;s Degree required.</li> <li> Cross-functional and/or similar experiences including field sales, finance, regulatory, research &amp; development and other relevant business functions, like Managed Care, MABI.</li> </ul> </div> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=749 http://pharmaboard.com/empid=749 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Scientist II, BioProcess Devel, Cell Culture <b>Experience:</b> 5 Year(s)<br/><b>Location:</b> California<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <div> <div id="description_box"> <div> <div> <div> &nbsp;</div> <div> &nbsp;</div> <p> &nbsp;</p> <p> Basic:</p> <p> &nbsp;</p> <ul> <li> Bachelors or Masters degree in chemical engineering, bioengineering, or a related field, with at least 7+(BS) or 5+(MS) years of experience</li> <li> Must have cell culture experience such as aseptic skill and bioreactor set up and sampling</li> <li> Demonstrated ability to independently design, execute and&nbsp;interpret critical experiments to answer scientific questions</li> <li> Has excellent attention to detail and ability to keep detailed written records in lab notebook.</li> <li> Able to work collaboratively within and outside of the group</li> <li> Has strong communication skills including verbal, written, and scientific data presentation.</li> <li> Has understanding of bioprocess engineering concepts</li> <li> Has proficiency with Microsoft Office software, ability to learn new software applications.</li> <li> Has strong planning and analytical skills</li> <li> Ability to multitask and work within timelines</li> </ul> <p> &nbsp;</p> <p> &nbsp;&nbsp;</p> <p> Preferred:</p> <p> &nbsp;</p> <ul> <li> Has hands on experience with monoclonal antibody or antibody-like molecule cell culture at GMP, pilot and/or laboratory scale</li> <li> Be proficient in operating cell culture analytical instruments such as CEDEX, ABL, ViCell, HPLC, etc.&nbsp;</li> </ul> <p> &nbsp;</p> <p> &nbsp;</p> </div> </div> </div> </div> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=748 http://pharmaboard.com/empid=748 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Sales Training Director <b>Experience:</b> 8 Year(s)<br/><b>Location:</b> Illinois<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <div> <font face="Arial"><font size="2">Responsibilities will impact approximately 100 employees across US Commercial.</font> </font></div> <div class="job_qualifications"> <div> <div> <font face="Arial" size="2"><font face="Arial" size="2">Bachelor&rsquo;s degree required.</font></font></div> <ul> <li> <font face="Arial" size="2"><font face="Arial" size="2">Knowledge of applicable regulations and standards affecting Pharmaceutical Products (e.g. CFR 210/211, cGMP) specifically, Operating Guidelines, PhRMA Guidelines, AbbVie Code of Business Conduct.</font></font></li> <li> <font face="Arial" size="2"><font face="Arial" size="2">8-10 years: combination of sales and sales training experience required.</font></font></li> <li> <font face="Arial" size="2"><font face="Arial" size="2">Sales management experience, at the District Manager level or above, required.</font></font></li> <li> <font face="Arial" size="2"><font face="Arial" size="2">Must have proven experience in identifying training needs and effectively addressing those needs.&nbsp;&nbsp; </font></font></li> <li> <font face="Arial" size="2"><font face="Arial" size="2">Must be able to communicate effectively and professionally with Commercial management and with cross-divisional teams</font></font></li> <li> <font face="Arial" size="2"><font face="Arial" size="2">Needs to have recent relevant commercial experience in the Oncology space, specifically hematology and or/solid tumor product and disease state experience</font></font></li> </ul> <div> <font face="Arial" size="2"><font face="Arial" size="2">&nbsp;</font><font face="Arial" size="2">Preferred:</font></font></div> <ul> <li> <font face="Arial" size="2"><font face="Arial" size="2">Master&rsquo;s degree or extensive experience in training &amp; development is preferred.</font></font></li> <li> <font face="Arial" size="2"><font face="Arial" size="2">Oncology Sales management experience, at the Regional Manager level or above preferred</font></font></li> <li> <font face="Arial" size="2"><font face="Arial" size="2">Oncology Marketing and/or Oncology Training experience at the Manager level or above also preferred</font></font></li> </ul> </div> </div> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=747 http://pharmaboard.com/empid=747 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com CRAs / Study Management Associates II&III <b>Experience:</b> 1 Year(s)<br/><b>Location:</b> California<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <div class="full_content"> <div class="main_content_box" id="description_box"> <div class="job_description"> <div class="job_qualifications"> <p style="margin-top:0px;margin-bottom:0px"> <font color="#000000" size="2">Position will be hired based on level of experience&nbsp;</font></p> <ul> <li> <div style="margin-bottom: 0px; margin-top: 0px;"> <font size="2"><b>Study Management Associate III:</b>&nbsp; Bachelor&rsquo;s Degree or equivalent is required, typically in nursing, medical&nbsp;or scientific field.&nbsp;&nbsp; An Associate&rsquo;s degree/R.N. or equivalent with relevant experience is acceptable; and 4+ years of pharmaceutical or biotech-related/clinical&nbsp;research related experience.&nbsp;</font></div> </li> <li> <div style="margin-bottom: 0px; margin-top: 0px;"> &nbsp;</div> </li> <li> <div style="margin-bottom: 0px; margin-top: 0px;"> <font size="2"><b>Study Management Associate II</b>:&nbsp; Bachelor&rsquo;s Degree or equivalent is required, typically in nursing, medical&nbsp;or scientific field.&nbsp;&nbsp; An Associate&rsquo;s degree/R.N. or equivalent with relevant experience is acceptable; and 1+ years of pharmaceutical or biotech-related/clinical&nbsp;research related experience</font></div> </li> <li> <div style="margin-bottom: 0px; margin-top: 0px;"> <font size="2">Demonstrate a high level of core and technical competencies through management of various components of clinical trials</font></div> </li> <li> <div style="margin-bottom: 0px; margin-top: 0px;"> <font size="2">Possess good communication skills and demonstrated leadership abilities</font></div> </li> <li> <div style="margin-bottom: 0px; margin-top: 0px;"> <font size="2">Competent in application of standard business procedures (SOPs, ICH-GCP, Global Regulations, Ethics and Compliance</font></div> </li> <li> <div style="margin-bottom: 0px; margin-top: 0px;"> <font size="2">Experience in study initiation through study completion is preferred.&nbsp;</font></div> </li> </ul> </div> </div> </div> </div> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=746 http://pharmaboard.com/empid=746 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Associate Director, QA Validation <b>Experience:</b> 8 Year(s)<br/><b>Location:</b> California<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <div> <font size="2"><b>Candidate must possess:</b></font></div> <ul> <li> <font size="2">B.S. or advanced degree in chemistry, biology or related science with &nbsp;minimum of 8 years of &nbsp;experience in the pharmaceutical / biopharmaceutical industry and 4 years of direct experience managing validation activities from a quality assurance perspective</font></li> <li> <font size="2">QA experience overseeing equipment/system, method and/or computer validation activities</font></li> <li> <font size="2">Experience with implementing and/or upgrading computerized systems</font></li> <li> <font size="2">Demonstrated working knowledge of current Good Manufacturing Practices (GMPs)</font></li> <li> <font size="2">Ability to lead others effectively on multi-disciplinary teams</font></li> <li> <font size="2">Experience with quality oversight of method transfers to external contract labs</font></li> <li> <font size="2">Excellent interpersonal skills, organizational skills and both written and verbal communication skills including the ability to influence collaborators in other departments</font></li> <li> <font size="2">Ability to operate in a fast-paced, multi-disciplinary industrial environment</font></li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=745 http://pharmaboard.com/empid=745 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Sen. Manager, Facilities & Engineering <b>Experience:</b> 10 Year(s)<br/><b>Location:</b> California<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <div class="full_content"> <div class="main_content_box" id="description_box"> <div class="job_description"> <div class="job_qualifications"> <p align="justify" class="BulletedList" style="margin: 0in 0in 0.0001pt; text-indent: 0in;"> <b><font size="2">Education, Qualification and Experience:</font></b></p> <p align="justify" class="BulletedList" style="margin: 0in 0in 0.0001pt; text-indent: 0in;"> &nbsp;</p> <ul> <li> <font size="2">Requires a Bachelor degree or equivalent number of years of experiences</font></li> <li> <font size="2">Must have at least 10+ years of experience in cGMP or regulated facilities</font></li> <li> <font size="2">Prior success in maintaining 100,000 plus feet facilities, including remodeling, moving and expansions.</font></li> <li> <font size="2">Demonstrated strong collaboration skills working with both internal and external organizations.</font></li> <li> <font size="2">Demonstrated capacity to skillfully communicate with all levels of employees as well as outside vendors and contractors.</font></li> <li> <font size="2">Must have experiences in lab and office built out construction projects.</font></li> <li> <font size="2">Must be results oriented with strong track record of success in delivering quality work space to employees.</font></li> <li> <font size="2">Strong interpersonal and communication skills (both written and verbal).</font></li> <li> <font size="2">Must be able to handle emergency and/or stressful situations.</font></li> <li> <font size="2">Prior experience facilities management in Biotech/Pharma industry preferred.</font></li> </ul> <p style="margin-top:0px;margin-bottom:0px"> &nbsp;</p> <div> <b style="margin: 0px; padding: 0px; border: 0px; font-variant-numeric: inherit; font-stretch: inherit; line-height: inherit; font-family: HelveticaNeueW01-55Roma, &quot;Helvetica Neue W01 55 Roman&quot;, &quot;Helvetica Neue&quot;, Helvetica, Arial, sans-serif; font-size: 13px; vertical-align: baseline; color: rgb(85, 85, 85); border-radius: 0px !important;"><font color="black" style="border-radius: 0px !important;"><font face="&quot;arial&quot;, &quot;sans-serif&quot;" style="border-radius: 0px !important;"><font size="9" style="border-radius: 0px !important;"><font size="2" style="border-radius: 0px !important;">Equal Opportunity Employer Minorities/Women/Veterans/Disabled</font></font></font></font></b></div> <div> &nbsp;</div> </div> </div> </div> </div> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=744 http://pharmaboard.com/empid=744 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Field Engineer <b>Experience:</b> 2 Year(s)<br/><b>Location:</b> Illinois<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <div class="full_content"> <div class="main_content_box" id="description_box"> <div class="job_description"> <br /> <div> &nbsp;</div> <div class="job_qualifications"> <div> <font size="2">Qualifications:</font></div> <div> &nbsp;</div> <div> <font size="2">Basic:</font></div> <ul> <li> <font face="Calibri"><font face="Arial" size="2">High School diploma or GED required.&nbsp; Associates Degree in electronics technology or equivalent is strongly desired.&nbsp; Minimum of two years&rsquo; experience as a Senior Instrument Technician or the equivalent.</font></font></li> <li> <font face="Calibri"><font face="Arial" size="2">Must manage activities to meet restrictive timelines.&nbsp; Must have skills in working with people, with good written and verbal communication skills.</font></font></li> <li> <font face="Calibri"><font face="Arial" size="2">Must possess knowledge of validated systems, applicable engineering standards and an ability to work with facility specific software applications is critical to the job function.</font></font></li> <li> <font face="Calibri"><font face="Arial" size="2">Ability to work within and promote a team environment.</font></font></li> </ul> <p style="MARGIN-BOTTOM: 0px; MARGIN-TOP: 0px"> <font face="Calibri"><font size="2"><strong>Equal Opportunity Employer Minorities/Women/Veterans/Disabled</strong></font></font></p> </div> </div> </div> </div> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=743 http://pharmaboard.com/empid=743 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Purchasing Specialist <b>Experience:</b> 2 Year(s)<br/><b>Location:</b> Illinois<br/><b>Industry Type:</b> BIO-1: Therapeutics<br/><b>Summary:</b> <div class="job details" id="content"> <div class="content_body block jPageContent" id="job_details_content"> <div class="jBlock"> <div class="full_content"> <div class="main_content_box" id="description_box"> <div class="job_description"> <div class="job_qualifications"> <div> <strong><font size="2">Qualifications</font></strong></div> <p style="MARGIN-BOTTOM: 0px; MARGIN-TOP: 0px"> <font size="2">Basic:</font></p> <ul> <li> <font size="2">Bachelor&rsquo;s degree or 4 years equivalent work experience</font></li> <li> <font size="2">A minimum of 2 years of procurement/negotiations experience in purchasing preferably but not limited to the pharmaceutical industry</font></li> <li> <font size="2">Strong knowledge of MS Excel, PowerPoint, Word and Outlook.</font></li> <li> <font size="2">Strong experience with writing RFX&rsquo;s.</font></li> <li> <font size="2">Solid experience conducting vendor negotiations.</font></li> <li> <font size="2">Ability to prioritize and organize workload across multiple project</font></li> <li> <font size="2">Proficient in Microsoft Word, Excel and PowerPoint. Possesses ability to learn and utilize other software tools as necessary</font></li> <li> <font size="2">Strong organizational skills required to coordinate and manage multiple cross divisional work process and projects</font></li> </ul> <div> &nbsp;</div> </div> </div> </div> </div> </div> </div> </div> <div id="container"> <div id="right_bar"> <div class="jBlockRegion block_region" data-area="right_column" data-page="job_details" id="right_holder"> <div class="block module bid-637" data-id="637" data-name="TEE_account_submissions"> <div class="capsule jBlock block_content" id="tee_account_submissions"> &nbsp;</div> </div> <div class="block module bid-639" data-id="639" data-name="top_referrer"> &nbsp;</div> <div class="block module bid-634" data-id="634" data-name="activity_feed"> &nbsp;</div> <div class="block module bid-642" data-id="642" data-name="similar_listings"> <div class="capsule jBlock block_content" id="similar_listings"> <div class="capsule_title"> <h2 class="font_header_bold"> &nbsp;</h2> </div> </div> </div> </div> </div> </div> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=742 http://pharmaboard.com/empid=742 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Senior Formulations Scientist <b>Experience:</b> 1 Year(s)<br/><b>Location:</b> Texas<br/><b>Industry Type:</b> Rx: Liquids / Topicals / Powders / Softgel<br/><b>Summary:</b> <div class="col-lg-9 col-md-9 col-sm-9 col-xs-12 job-detail-input dhtml_editor_render " id="job_details_ats_requisition_requirements"> <p> <strong>EDUCATION and/or EXPERIENCE</strong></p> <ol> <li> <p style="margin-top: 0in; margin-bottom: 0pt;"> Degree in Chemistry, Biology or related field from a four-year college or university is required.</p> </li> <li> <p> Minimum 1 &ndash; 3 years of related experience is required for Ph.D., 4 &ndash; 6 years for Master&rsquo;s degree, 7 &ndash; 9 years for Bachelor&rsquo;s degree.Experience in formulation of pharmaceutical biological products is required.Knowledge in pharmaceutical drug development in semi-solids dosage forms and/or new drug delivery systems is a must.</p> </li> <li> <p> Strong knowledge of regulatory requirements and cGMPs is a must.</p> </li> <li> <p> Must be able to organize and prioritize work in order to accomplish tasks assigned.</p> </li> <li> <p> Ability to develop advanced research protocols, present findings and analyze, evaluate and interpret data.</p> </li> <li> <p> Strong proficiency in computer, writing reports, laboratory, analytical, and organizational skills.</p> </li> <li> <p> Must have excellent communication skills, a demonstrated ability to work with diverse teams and manage multiple projects within aggressive timelines.Ability to interact with personnel at all levels in department.</p> </li> </ol> </div> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=740 http://pharmaboard.com/empid=740 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com QC Inspectors <b>Experience:</b> 0 Year(s)<br/><b>Location:</b> Pennsylvania<br/><b>Industry Type:</b> Rx: Solid Dose / Tablets / Capsules<br/><b>Summary:</b> <ul class="WF0M WM0M" role="presentation"> <li class="WL-M" role="presentation"> <div class="WP-M"> <div class="WE-H WF-H"> <div aria-invalid="false" aria-labelledby="richTextArea.jobPosting.jobDescription-input--uid23-input-formLabel" class="WEYV WI-V WAYV WH-V WN3 WFYV" data-automation-id="richTextEditor" id="richTextArea.jobPosting.jobDescription-input--uid23-input"> <div class="GWTCKEditor-Disabled" dir="ltr"> <p> &nbsp;you like wild growth and working with happy, enthusiastic over-achievers, you&#39;ll enjoy your career with us!</p> </div> </div> </div> </div> </li> </ul> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=739 http://pharmaboard.com/empid=739 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com QC Insprectors <b>Experience:</b> 1 Year(s)<br/><b>Location:</b> Pennsylvania<br/><b>Industry Type:</b> Rx: Solid Dose / Tablets / Capsules<br/><b>Summary:</b> <ul class="WF0M WM0M" role="presentation"> <li class="WL-M" role="presentation"> <div class="WP-M"> <div class="WE-H WF-H"> <div aria-invalid="false" aria-labelledby="richTextArea.jobPosting.jobDescription-input--uid23-input-formLabel" class="WEYV WI-V WAYV WH-V WN3 WFYV" data-automation-id="richTextEditor" id="richTextArea.jobPosting.jobDescription-input--uid23-input"> <div class="GWTCKEditor-Disabled" dir="ltr"> <p> If you like wild growth and working with happy, enthusiastic over-achievers, you&#39;ll enjoy your career with us!</p> <p> &nbsp;</p> </div> </div> </div> </div> </li> </ul> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=738 http://pharmaboard.com/empid=738 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Inside Sales Representative <b>Experience:</b> 3 Year(s)<br/><b>Location:</b> Pennsylvania<br/><b>Industry Type:</b> Rx: Solid Dose / Tablets / Capsules<br/><b>Summary:</b> <ul class="WF0M WM0M" role="presentation"> <li class="WL-M" role="presentation"> <div class="WP-M"> <div class="WE-H WF-H"> <div aria-invalid="false" aria-labelledby="richTextArea.jobPosting.jobDescription-input--uid65-input-formLabel" class="WEYV WI-V WAYV WH-V WN3 WFYV" data-automation-id="richTextEditor" id="richTextArea.jobPosting.jobDescription-input--uid65-input"> <div class="GWTCKEditor-Disabled" dir="ltr"> <ul> <li> B.S degree or equivalent work experience.</li> </ul> <ul> <li> Minimum of 3 years of marketing and/or inside sales experience.</li> <li> Outstanding communication and interpersonal skills; professional telephone and email communication are required.</li> </ul> <ul> <li> Marketing experience is a plus.</li> <li> Knowledge of clinical trials, research services, drug development, or IRT a plus.</li> <li> Strong computer skills and proficiency with Microsoft Office Suite. &nbsp;Prior experience with Salesforce a plus.</li> <li> Ability to work with minimal supervision and in a team environment.</li> </ul> </div> </div> </div> </div> </li> </ul> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=737 http://pharmaboard.com/empid=737 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Buyer <b>Experience:</b> 5 Year(s)<br/><b>Location:</b> Pennsylvania<br/><b>Industry Type:</b> Rx: Solid Dose / Tablets / Capsules<br/><b>Summary:</b> <ul class="WF0M WM0M" role="presentation"> <li class="WL-M" role="presentation"> <div class="WP-M"> <div class="WE-H WF-H"> <div aria-invalid="false" aria-labelledby="richTextArea.jobPosting.jobDescription-input--uid34-input-formLabel" class="WEYV WI-V WAYV WH-V WN3 WFYV" data-automation-id="richTextEditor" id="richTextArea.jobPosting.jobDescription-input--uid34-input"> <div class="GWTCKEditor-Disabled" dir="ltr"> <p dir="LTR"> <b>EDUCATION and/or EXPERIENCE:</b></p> <p dir="LTR"> Bachelor&rsquo;s degree (B.A.) from four-year college or university or equivalent experience. Minimum 5 years in purchasing function.</p> </div> </div> </div> </div> </li> </ul> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=736 http://pharmaboard.com/empid=736 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Tech Transfer Professional <b>Experience:</b> 0 Year(s)<br/><b>Location:</b> Pennsylvania<br/><b>Industry Type:</b> Rx: Solid Dose / Tablets / Capsules<br/><b>Summary:</b> <div class="WP0M" style="width: 65%;"> <div class="WN3" id="wd-PageContent-vbox"> <div class="WK1M"> <ul class="WF0M WM0M" role="presentation"> <li class="WL-M" role="presentation"> <div class="WN-M"> &nbsp;</div> <div class="WP-M"> <div class="WE-H"> <div class="WJMV WN3 WKNV" data-automation-id="responsiveMonikerInput" id="labeledImage.LOCATION--uid120"> <div class="WOMV"> <ul class="WOEP WNMV" data-automation-id="selectedItemList" role="list" tabindex="-2"> <li class="WCFP" role="presentation"> <div aria-label="Allentown, press delete to clear value." aria-posinset="1" aria-setsize="1" class="WIEP WBFP" data-automation-id="menuItem" id="b5dc7ad832294a47b6f1c24c275bae50" role="listitem" tabindex="-2"> <div class="WJEP"> <div class="WPJN"> <ul class="WDJN WIJN" role="presentation"> <li class="WOJN"> <div aria-labelledby="promptOption-gwt-uid-312" class="WKIJ WJIJ WBJJ WAWP WHVP" data-automation-id="LOCATION_charm" role="presentation"> <svg class="wd-icon-location wd-icon" focusable="false" height="24" role="presentation" viewbox="0 0 24 24" width="24" xmlns="http://www.w3.org/2000/svg"><path class="wd-icon-container wd-icon-fill" d="M 12 2 c 3.866 0 7 2.98 7 6.657 C 19 12.333 13 22 12 22 S 5 12.333 5 8.657 C 5 4.98 8.134 2 12 2 Z m 0 11.111 c 2.577 0 4.667 -1.99 4.667 -4.444 c 0 -2.455 -2.09 -4.445 -4.667 -4.445 s -4.667 1.99 -4.667 4.445 c 0 2.454 2.09 4.444 4.667 4.444 Z" fill-rule="evenodd"></path> </svg></div> </li> </ul> <div aria-label="Allentown" aria-labelledby="labeledImage.LOCATION--uid120-formLabel" class="gwt-Label WAKN" data-automation-id="promptOption" data-automation-label="Allentown" id="promptOption-gwt-uid-312" title="Allentown"> Allentown</div> <ul class="WDJN"> </ul> </div> </div> </div> </li> </ul> </div> </div> </div> </div> </li> </ul> <div class="WP0M"> <div class="WN3" id="wd-HBox-NO_METADATA_ID"> <ul class="WLKL" data-automation-id="buttonBar"> <li class="WMKL"> <div aria-hidden="false" class="WHBM WN3" data-automation-id="dropDownCommandButton" id="wd-DropDownCommandButton-commandButton.siteLabels['POSTING.Apply_Button']"> <button aria-disabled="false" class="WERL WIRL WIYM WEBM WHSL" data-automation-activebutton="true" data-automation-button-type="SECONDARY" data-automation-id="label" data-automation-task-ids="VIEW_TASK_TaskId" role="button" tabindex="0" title="Apply" type="button"><span class="WGRL" title="Apply">Apply</span></button><button aria-disabled="true" aria-expanded="false" aria-hidden="true" class="WERL WIYM WGBM WHSL WHRL" data-automation-activebutton="false" data-automation-button-type="SECONDARY" data-automation-id="dropdownArrow" role="button" style="display: none;" tabindex="-2" type="button"></button></div> </li> <li class="WMKL"> <div aria-hidden="false" class="WHBM WN3" data-automation-id="dropDownCommandButton" id="wd-DropDownCommandButton-commandButton.siteLabels['APPLY.MY_EXPERIENCE.Import_from_LinkedIn']"> <button aria-disabled="false" class="WERL WIRL WIYM WEBM WEQL" data-automation-activebutton="true" data-automation-button-type="AUXILIARY" data-automation-id="label" data-automation-task-ids="VIEW_TASK_TaskId" role="button" tabindex="0" title="Apply with LinkedIn" type="button"><span class="WGRL" title="Apply with LinkedIn">Apply with LinkedIn</span></button><button aria-disabled="true" aria-expanded="false" aria-hidden="true" class="WERL WIYM WGBM WEQL WHRL" data-automation-activebutton="false" data-automation-button-type="AUXILIARY" data-automation-id="dropdownArrow" role="button" style="display: none;" tabindex="-2" type="button"></button></div> </li> </ul> </div> </div> <ul class="WF0M WM0M" role="presentation"> <li class="WL-M" role="presentation"> <div class="WN-M"> &nbsp;</div> <div class="WP-M"> <div class="WE-H WF-H"> <div aria-invalid="false" aria-labelledby="richTextArea.jobPosting.jobDescription-input--uid121-input-formLabel" class="WEYV WI-V WAYV WH-V WN3 WFYV" data-automation-id="richTextEditor" id="richTextArea.jobPosting.jobDescription-input--uid121-input"> <div aria-hidden="true" style="display: none;"> <textarea class="gwt-TextArea" data-automation-id="richTextHiddenTextArea" name="gwt-uid-317"></textarea></div> <div class="GWTCKEditor-Disabled" dir="ltr"> <p dir="LTR"> Provide Quality guidance in the support and transfer of all new projects initiated to Sharp.&nbsp; Using Quality Engineering concepts and working closely with clients and internal staff at all levels of the organization, create Critical to Quality attributes to ensure successful transfer of projects into the manufacturing environment for first time pass success.&nbsp; Working closely with the&nbsp; Project teams and Client representatives, determine and establish client <span class="WNNY ">requirements/expectations</span> to address internal and external quality issues using problem solving and root cause analysis techniques.&nbsp; Responsible for ongoing communication with internal departments concerning compliance with cGMP and customer requirements, and new projects.&nbsp; Review and approve all Master Packaging Records, qualification and validation documents pre/post execution.&nbsp;</p> <p dir="DEFAULT" style="text-align: inherit;"> &nbsp;</p> <p dir="LTR"> Scope of the position includes Allentown and Conshohocken. The impact of decisions relating to customer interface, quality inspections, and documentation requirements could expose the company to significant risk or economic loss.</p> <p dir="DEFAULT" style="text-align: inherit;"> &nbsp;</p> <p dir="LTR"> <b>ESSENTIAL DUTIES AND RESPONSIBILITIES: </b>The all-inclusive list of responsibilities may be distributed to multiple Associates.&nbsp; Other duties may also be assigned.</p> <p dir="DEFAULT" style="text-align: inherit;"> &nbsp;</p> <p dir="LTR"> Promotes a team based culture of open transparency and collaboration to stimulate communication and enhance morale.</p> <p dir="DEFAULT" style="text-align: inherit;"> &nbsp;</p> <p dir="LTR"> Be the Quality Subject Matter Expert on all project teams in regards to incoming inspection, in-process inspection and documentation requirements.</p> <p dir="DEFAULT" style="text-align: inherit;"> &nbsp;</p> <p dir="LTR"> Provide Quality oversight for the onboarding of new projects (products / processes) within their respective Center of Excellence.&nbsp; Establish the critical to quality elements for these new projects.</p> <p dir="DEFAULT" style="text-align: inherit;"> &nbsp;</p> <p dir="LTR"> Responsible to review and approve Master Packaging Records and Validation protocols for the respective project within their Center of Excellence.</p> <p dir="DEFAULT" style="text-align: inherit;"> &nbsp;</p> <p dir="LTR"> Responsible for providing status updates to customer regarding events/deviations, completed batch records, change controls, complaints, temporary change controls, Master Packaging Records, Quality Agreements and validation protocols within their COE.</p> <p dir="DEFAULT" style="text-align: inherit;"> &nbsp;</p> <p dir="LTR"> Assist in appropriate problem solving initiatives to address customer or regulatory quality issues as requested by Senior Management.</p> <p dir="DEFAULT" style="text-align: inherit;"> &nbsp;</p> <p dir="LTR"> Participate in process improvement initiatives driven by the business and industry.</p> <p dir="DEFAULT" style="text-align: inherit;"> &nbsp;</p> <p dir="LTR"> <b>SUPERVISORY RESPONSIBILITIES: </b></p> <p dir="LTR"> No supervisory responsibilities.</p> <p dir="DEFAULT" style="text-align: inherit;"> &nbsp;</p> <p dir="LTR"> <b>QUALIFICATIONS: </b></p> <p dir="LTR"> To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</p> <p dir="DEFAULT" style="text-align: inherit;"> &nbsp;</p> <p dir="LTR"> <b>EDUCATION and/or EXPERIENCE: </b></p> <p dir="LTR"> Bachelor&rsquo;s degree in Engineering or Science (BS/BA) is preferred with one to three years of related experience and/or training.</p> <p dir="LTR"> Associates degree in Engineering or Science (BS/BA) is required with four to six years of related experience and/or training.</p> <p dir="LTR"> Outside certification of basic quality skills and practices (i.e. ASQ CQIA, CQPA, etc.) is desired.</p> <p dir="LTR"> - Experience in inspection of pharmaceutical or related industry is required.</p> <p dir="LTR"> - General Knowledge of FDA regulations related to cGMP&rsquo;s is required.</p> <p dir="LTR"> - General knowledge of quality control/assurance is required.</p> <p dir="LTR"> - Good documentation and communication skills are required.</p> <p dir="LTR"> - Good organizational and planning skills are required.</p> <p dir="LTR"> - Ability to multi-task is required.</p> <p dir="DEFAULT" style="text-align: inherit;"> &nbsp;</p> <p dir="LTR"> <b>LANGUAGE SKILLS: </b></p> <p dir="LTR"> Ability to read and interpret documents such as compliance regulations, validation protocols, standard operating procedures, safety rules, operating and maintenance instructions and technical manuals. Ability to write detailed technical reports.&nbsp;</p> <p dir="DEFAULT" style="text-align: inherit;"> &nbsp;</p> <p dir="LTR"> - Internal: Frequent contact with Quality, Operations, Engineering, Project Management employees for information exchange, collaboration, problem solving, direction regarding customer quality issues and cGMP issues.</p> <p dir="DEFAULT" style="text-align: inherit;"> &nbsp;</p> <p dir="LTR"> - External: Frequent contact with customer representatives planning new product introductions, addressing technical agreements and problem solving quality issues specific to the site.</p> </div> </div> </div> </div> </li> </ul> </div> </div> </div> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=735 http://pharmaboard.com/empid=735 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com QC Supervisor <b>Experience:</b> 5 Year(s)<br/><b>Location:</b> Pennsylvania<br/><b>Industry Type:</b> Rx: Solid Dose / Tablets / Capsules<br/><b>Summary:</b> <p dir="LTR"> <b>QUALIFICATIONS</b></p> <p dir="LTR"> To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.</p> <ul> <li> Bachelor&rsquo;s degree in Science (BS/BA) from a four-year college or university preferred; or five&nbsp;to <span class="WNNY ">seven&nbsp;years-related</span> pharmaceutical experience and training; or equivalent combination of education and experience.</li> <li> Minimum of two years supervisory experience.</li> <li> Knowledge of FDA regulations including cGMPs and current industry practice</li> <li> Thorough knowledge of quality control/assurance and/or operations</li> <li> Experience with investigational drugs and clinical supply operations</li> <li> Good written and oral communication skills</li> <li> Good organizational and planning skills</li> <li> Strong attention to detail</li> <li> Strong working knowledge of personal computers and Microsoft Office Products, including Word, Project and Excel.</li> </ul> <p dir="DEFAULT" style="text-align:inherit"> &nbsp;</p> <p dir="LTR"> <b>MANAGER REPSONSIBILITIES</b></p> <p dir="LTR"> Direct supervision of quality control inspectors.&nbsp; Carry out supervisory responsibilities in accordance with the organization&#39;s policies and applicable laws. Responsibilities include interviewing, hiring, and training employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems.</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=734 http://pharmaboard.com/empid=734 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com QA Supervisor <b>Experience:</b> 1 Year(s)<br/><b>Location:</b> Pennsylvania<br/><b>Industry Type:</b> Rx: Solid Dose / Tablets / Capsules<br/><b>Summary:</b> <p dir="LTR"> <b>EDUCATION and/or EXPERIENCE: </b></p> <p dir="LTR"> High School Degree with College credits/degree preferred; or one to two years related experience and/or training; or equivalent combination of education and experience. Experience in pharmaceutical or related industry is desired.</p> <p dir="LTR"> - Knowledge of FDA regulations including cGMP&rsquo;s and current industry practice</p> <p dir="LTR"> - Thorough knowledge of quality control/assurance and/or operations</p> <p dir="LTR"> - Knowledge of DEA regulations</p> <p dir="LTR"> - Broad knowledge of current pharmaceutical industry including packaging practices</p> <p dir="LTR"> - Good written and oral communication skills</p> <p dir="LTR"> - Good organizational and planning skills</p> <p dir="DEFAULT" style="text-align:inherit"> &nbsp;</p> <p dir="LTR"> <b>MATHEMATICAL SKILLS: </b></p> <p dir="LTR"> Ability to apply mathematical operations to such tasks as they apply to the pharmaceutical industry.&nbsp; This includes evaluation of statistical sampling plans.</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=733 http://pharmaboard.com/empid=733 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Production Planner <b>Experience:</b> 2 Year(s)<br/><b>Location:</b> Pennsylvania<br/><b>Industry Type:</b> Rx: Solid Dose / Tablets / Capsules<br/><b>Summary:</b> <p dir="LTR"> <b>EDUCATION and/or EXPERIENCE: </b></p> <p dir="LTR"> Bachelor&rsquo;s degree in business, supply chain, project management, operations or related fields, Associates and two years of business experience, and/or combination of relevant education and industry experience.</p> <p dir="LTR"> MRP knowledge required.&nbsp; APICS Certification preferable.&nbsp;</p> <p dir="LTR"> Experience working in an FDA and DEA regulated environment is desirable.</p> <p dir="DEFAULT" style="text-align:inherit"> &nbsp;</p> <p dir="LTR"> <b>COMPUTER SKILLS: </b></p> <p dir="LTR"> Knowledge of Microsoft Office Suite including Word, Excel and Project.&nbsp; Familiar with MRP systems.</p> <p dir="DEFAULT" style="text-align:inherit"> &nbsp;</p> <p dir="LTR"> <b>LANGUAGE SKILLS: </b></p> <p dir="LTR"> Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.&nbsp; Ability to write routine reports and <span class="WNNY ">correspondence.&nbsp;</span> Ability to speak clearly and effectively before groups of customers or employees of organization.</p> <p dir="DEFAULT" style="text-align:inherit"> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=732 http://pharmaboard.com/empid=732 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Validation Manager <b>Experience:</b> 0 Year(s)<br/><b>Location:</b> Pennsylvania<br/><b>Industry Type:</b> Rx: Solid Dose / Tablets / Capsules<br/><b>Summary:</b> <p dir="LTR"> <b>EDUCATION and/or EXPERIENCE:</b></p> <p dir="LTR"> Bachelor&rsquo;s degree in technical discipline (BS/BA) from a four-year college or university preferred with five to ten years related experience and or training; or equivalent combination of education and experience.&nbsp; Independent certification of advanced quality skills and practices (i.e. ASQ, CQE, Six Sigma, etc.) is desired.</p> <ul> <li> Broad knowledge of current validation principles and industry practices including FDA regulations, cGMPs, and validation guidance documents is required.</li> <li> Familiar with quality engineering practices in manufacturing operations is required.</li> <li> Knowledge of basic engineering principles and practices, equipment automation controls, etc. is required.</li> <li> Familiarity with quality variable and attribute sampling plans (e.g. ANSI ZI.4) is required.</li> <li> Ability to multi-task is required.</li> <li> Ability to independently plan and schedule validation activities.</li> <li> Proven ability to commit to and meet project deadlines is required.</li> <li> Good written and oral communication skills are required.</li> <li> Good organizational and planning skills are required.</li> </ul> <p dir="DEFAULT" style="text-align:inherit"> &nbsp;</p> <p dir="LTR"> <b>MATHEMATICAL SKILLS: </b></p> <p dir="LTR"> Basic math skills (addition, subtraction, multiplication and division) are required.&nbsp; Ability to apply complex &nbsp;mathematical operations, scientific notation, and conversion factors.&nbsp; Advanced understanding of statistics including, but not limited to standard deviation, regression, distribution analysis, capability analysis, trend analysis, sampling theory, and Design of Experiments (DOE).&nbsp;&nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=731 http://pharmaboard.com/empid=731 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Multiple Sales Positions Nationwide <b>Experience:</b> 3 Year(s)<br/><b>Location:</b> New Jersey<br/><b>Industry Type:</b> Rx: Solid Dose / Tablets / Capsules<br/><b>Summary:</b> <blockquote style="margin: 0 0 0 40px; border: none; padding: 0px;"> <p class="msonormal"> <font face="Times New Roman" size="3"><b><span>&nbsp;</span></b><b><u><span>Healthcare Sales Professionals:</span></u></b></font></p> </blockquote> <ul style="list-style-position: inside; margin-top: 0px; margin-left: 0px; padding-top: 0px; padding-left: 0px;"> <li> <ul> <li class="msolistparagraph" style="text-indent: -18px;"> <font face="Times New Roman" size="3">4 year Bachelor degree (or equivalent) from an accredited University required</font></li> <li class="msolistparagraph" style="text-indent: -18px;"> <font face="Times New Roman" size="3">2-4 years&rsquo; experience selling Pharmaceutical products required</font></li> <li class="msolistparagraph" style="text-indent: -18px;"> <font face="Times New Roman" size="3">Launch Experience with Pharmaceutical products a strong plus</font></li> <li class="msolistparagraph" style="text-indent: -18px;"> <font face="Times New Roman" size="3">Must have been in top 25% of current sales team (and/or President&rsquo;s Club) for at least one of the last three years</font></li> <li class="msolistparagraph" style="text-indent: -18px;"> <font face="Times New Roman" size="3">Demonstrate the following: work ethic and integrity; planning, organizing and territory management skills; strong interpersonal skills; excellent communication skills; critical thinking and analysis; problem solving; decisiveness; sound judgement; customer-focused selling skills; basic computer skills; ability to listen and learn.</font></li> </ul> </li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=730 http://pharmaboard.com/empid=730 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Sen. Medical Science Liaison / MSL <b>Experience:</b> 3 Year(s)<br/><b>Location:</b> New Jersey<br/><b>Industry Type:</b> Rx: Solid Dose / Tablets / Capsules<br/><b>Summary:</b> <p class="msonormal" style="margin-bottom:0px;margin-bottom:0.00013333333333333334px;line-height: normal;tab-stops:61.06666666666666px 122.13333333333333px 183.2px 244.26666666666665px 305.3333333333333px 366.4px 427.4666666666667px 488.5333333333333px 549.5999999999999px 610.6666666666666px 671.7333333333333px 732.8px 793.8666666666666px 854.9333333333334px 916px 977.0666666666666px"> <span style="font-family: Arial, sans-serif;"><font size="3"><b>Qualifications:</b></font></span></p> <p class="msonormal" style="margin-bottom:0px;margin-bottom:0.00013333333333333334px;line-height: normal;tab-stops:61.06666666666666px 122.13333333333333px 183.2px 244.26666666666665px 305.3333333333333px 366.4px 427.4666666666667px 488.5333333333333px 549.5999999999999px 610.6666666666666px 671.7333333333333px 732.8px 793.8666666666666px 854.9333333333334px 916px 977.0666666666666px"> <b><span style="font-family: Arial, sans-serif;">&nbsp;</span></b></p> <ul style="list-style-position: inside; margin-top: 0px; margin-left: 0px; padding-top: 0px; padding-left: 0px;"> <li class="msolistparagraphcxspfirst" style="margin-bottom:0px;margin-bottom:0.00013333333333333334px; text-indent:-18px;line-height:normal; tab-stops:61.06666666666666px 122.13333333333333px 183.2px 244.26666666666665px 305.3333333333333px 366.4px 427.4666666666667px 488.5333333333333px 549.5999999999999px 610.6666666666666px 671.7333333333333px 732.8px 793.8666666666666px 854.9333333333334px 916px 977.0666666666666px"> <font size="3"><span style="font-family: Arial, sans-serif;">Advanced degree in medical/biosciences (e.g. M.D., PhD, PharmD, DPH, EdD, etc.)</span></font></li> <li class="msolistparagraphcxspmiddle" style="margin-bottom:0px;margin-bottom: 0.00013333333333333334px;text-indent:-18px;line-height:normal; tab-stops:61.06666666666666px 122.13333333333333px 183.2px 244.26666666666665px 305.3333333333333px 366.4px 427.4666666666667px 488.5333333333333px 549.5999999999999px 610.6666666666666px 671.7333333333333px 732.8px 793.8666666666666px 854.9333333333334px 916px 977.0666666666666px"> <font size="3"><span style="font-family: Arial, sans-serif;">Minimum of 3 years of MSL experience required. <span>&nbsp;</span></span></font></li> <li class="msolistparagraphcxspmiddle" style="margin-bottom:0px;margin-bottom: 0.00013333333333333334px;text-indent:-18px;line-height:normal; tab-stops:61.06666666666666px 122.13333333333333px 183.2px 244.26666666666665px 305.3333333333333px 366.4px 427.4666666666667px 488.5333333333333px 549.5999999999999px 610.6666666666666px 671.7333333333333px 732.8px 793.8666666666666px 854.9333333333334px 916px 977.0666666666666px"> <font size="3"><span style="font-family: Arial, sans-serif;">Experience in CNS/Psychiatry therapeutic area preferred.</span></font></li> <li class="msolistparagraphcxspmiddle" style="margin-bottom:0px;margin-bottom: 0.00013333333333333334px;text-indent:-18px;line-height:normal; tab-stops:61.06666666666666px 122.13333333333333px 183.2px 244.26666666666665px 305.3333333333333px 366.4px 427.4666666666667px 488.5333333333333px 549.5999999999999px 610.6666666666666px 671.7333333333333px 732.8px 793.8666666666666px 854.9333333333334px 916px 977.0666666666666px"> <font size="3"><span style="font-family: Arial, sans-serif;">Experience in ADHD therapeutic area preferred.</span></font></li> <li class="msolistparagraphcxspmiddle" style="margin-bottom:0px;margin-bottom: 0.00013333333333333334px;text-indent:-18px;line-height:normal; tab-stops:61.06666666666666px 122.13333333333333px 183.2px 244.26666666666665px 305.3333333333333px 366.4px 427.4666666666667px 488.5333333333333px 549.5999999999999px 610.6666666666666px 671.7333333333333px 732.8px 793.8666666666666px 854.9333333333334px 916px 977.0666666666666px"> <font size="3"><span style="font-family: Arial, sans-serif;">Strong broad-based scientific and pharmaceutical knowledge as well as excellent presentation and teaching skills required.<span>&nbsp; </span></span></font></li> <li class="msolistparagraphcxspmiddle" style="margin-bottom:0px;margin-bottom: 0.00013333333333333334px;text-indent:-18px;line-height:normal; tab-stops:61.06666666666666px 122.13333333333333px 183.2px 244.26666666666665px 305.3333333333333px 366.4px 427.4666666666667px 488.5333333333333px 549.5999999999999px 610.6666666666666px 671.7333333333333px 732.8px 793.8666666666666px 854.9333333333334px 916px 977.0666666666666px"> <font size="3"><span style="font-family: Arial, sans-serif;">Strong overall written and verbal communication skills required.<span>&nbsp; </span></span></font></li> <li class="msolistparagraphcxspmiddle" style="margin-bottom:0px;margin-bottom: 0.00013333333333333334px;text-indent:-18px;line-height:normal; tab-stops:61.06666666666666px 122.13333333333333px 183.2px 244.26666666666665px 305.3333333333333px 366.4px 427.4666666666667px 488.5333333333333px 549.5999999999999px 610.6666666666666px 671.7333333333333px 732.8px 793.8666666666666px 854.9333333333334px 916px 977.0666666666666px"> <font size="3"><span style="font-family: Arial, sans-serif;">Excellent level of experience and confidence speaking about drug information/disease state treatment required.</span></font></li> <li class="msolistparagraphcxspmiddle" style="margin-bottom:0px;margin-bottom: 0.00013333333333333334px;text-indent:-18px;line-height:normal; tab-stops:61.06666666666666px 122.13333333333333px 183.2px 244.26666666666665px 305.3333333333333px 366.4px 427.4666666666667px 488.5333333333333px 549.5999999999999px 610.6666666666666px 671.7333333333333px 732.8px 793.8666666666666px 854.9333333333334px 916px 977.0666666666666px"> <font size="3"><span style="font-family: Arial, sans-serif;">Excellent working knowledge of the pharmaceutical corporate environment and appreciation for Commercial Operations, including Marketing and Sales strategies required.</span></font></li> <li class="msolistparagraphcxspmiddle" style="margin-bottom:0px;margin-bottom: 0.00013333333333333334px;text-indent:-18px;line-height:normal; tab-stops:61.06666666666666px 122.13333333333333px 183.2px 244.26666666666665px 305.3333333333333px 366.4px 427.4666666666667px 488.5333333333333px 549.5999999999999px 610.6666666666666px 671.7333333333333px 732.8px 793.8666666666666px 854.9333333333334px 916px 977.0666666666666px"> <font size="3"><span style="font-family: Arial, sans-serif;">Excellent working knowledge of relevant regulatory and compliance issues related to the MSL role required.</span></font></li> <li class="msolistparagraphcxspmiddle" style="margin-bottom:0px;margin-bottom: 0.00013333333333333334px;text-indent:-18px;line-height:normal; tab-stops:61.06666666666666px 122.13333333333333px 183.2px 244.26666666666665px 305.3333333333333px 366.4px 427.4666666666667px 488.5333333333333px 549.5999999999999px 610.6666666666666px 671.7333333333333px 732.8px 793.8666666666666px 854.9333333333334px 916px 977.0666666666666px"> <font size="3"><span style="font-family: Arial, sans-serif;">Ability to influence without direct authority required.</span></font></li> <li class="msolistparagraphcxspmiddle" style="margin-bottom:0px;margin-bottom: 0.00013333333333333334px;text-indent:-18px;line-height:normal; tab-stops:61.06666666666666px 122.13333333333333px 183.2px 244.26666666666665px 305.3333333333333px 366.4px 427.4666666666667px 488.5333333333333px 549.5999999999999px 610.6666666666666px 671.7333333333333px 732.8px 793.8666666666666px 854.9333333333334px 916px 977.0666666666666px"> <font size="3"><span style="font-family: Arial, sans-serif;">Proven track record of establishing, maintaining, and enhancing effective and successful collegial relationships with key opinion leaders (KOLs) in therapeutic areas of interest required.</span></font></li> <li class="msolistparagraphcxspmiddle" style="margin-bottom:0px;margin-bottom: 0.00013333333333333334px;text-indent:-18px;line-height:normal; tab-stops:61.06666666666666px 122.13333333333333px 183.2px 244.26666666666665px 305.3333333333333px 366.4px 427.4666666666667px 488.5333333333333px 549.5999999999999px 610.6666666666666px 671.7333333333333px 732.8px 793.8666666666666px 854.9333333333334px 916px 977.0666666666666px"> <font size="3"><span style="font-family: Arial, sans-serif;">Experience and knowledge of government and private payer relationships and direct experience in a payer environment preferred.</span></font></li> <li class="msolistparagraphcxsplast" style="margin-bottom:0px;margin-bottom:0.00013333333333333334px; text-indent:-18px;line-height:normal; tab-stops:61.06666666666666px 122.13333333333333px 183.2px 244.26666666666665px 305.3333333333333px 366.4px 427.4666666666667px 488.5333333333333px 549.5999999999999px 610.6666666666666px 671.7333333333333px 732.8px 793.8666666666666px 854.9333333333334px 916px 977.0666666666666px"> <font size="3"><span style="font-family: Arial, sans-serif;">Ability to travel 60 &ndash; 70% in assigned geography required.<span>&nbsp;&nbsp;</span></span></font></li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=729 http://pharmaboard.com/empid=729 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Associate Director, Sourcing & Procurement <b>Experience:</b> 10 Year(s)<br/><b>Location:</b> New Jersey<br/><b>Industry Type:</b> Rx: Solid Dose / Tablets / Capsules<br/><b>Summary:</b> <p class="msonormal"> <b>Job Qualifications:</b></p> <p class="msonormal"> <b>&nbsp;</b></p> <p class="msonormal"> <font size="3">&bull;<span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span>Bachelor&rsquo;s Degree required.<span>&nbsp; </span>MBA preferred.<span>&nbsp; </span>Minimum 10 years&rsquo; progressive experience in procurement in the pharmaceutical industry required.</font></p> <p class="msonormal"> <font size="3">&bull;<span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span>CPM and/or CPIM certification preferred.</font></p> <p class="msonormal"> <font size="3">&bull;<span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span>Strong hands-on knowledge and skills with JD Edwards system, MS Excel, MS Word, MS Project preferred.</font></p> <p class="msonormal"> <font size="3">&bull;<span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span>Effective communication skills to work professionally with internal and external personnel at all levels required.</font></p> <p class="msonormal"> <font size="3">&bull;<span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span>Demonstrated strong analytical and communications skills required.</font></p> <p class="msonormal"> <font size="3">&bull;<span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span>Ability to manage multiple complex projects and effectively utilize, supervise, and train staff required.</font></p> <p class="msonormal"> <font size="3">&bull;<span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span>Assertiveness and perseverance to overcome obstacles tactfully but effectively required.</font></p> <p class="msonormal"> <font size="3">&bull;<span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span>Ability to travel up to 30% required.</font></p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=727 http://pharmaboard.com/empid=727 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com QC Chemist <b>Experience:</b> 1 Year(s)<br/><b>Location:</b> New Jersey<br/><b>Industry Type:</b> Rx: Solid Dose / Tablets / Capsules<br/><b>Summary:</b> <blockquote style="margin: 0 0 0 40px; border: none; padding: 0px;"> <p class="msonormal" style="margin-bottom:0px;margin-bottom:0.00013333333333333334px;line-height: normal"> <span><span><font face="Times New Roman" size="4"><b>Qualifications:</b></font></span></span></p> <p class="msonormal" style="margin-bottom:0px;margin-bottom:0.00013333333333333334px;line-height: normal"> &nbsp;</p> </blockquote> <ul style="margin-top:0px" type="disc"> <li> <ul> <li class="msonormal" style="margin-top:4px;"> <span style="line-height: 115%;"><font face="Times New Roman" size="4">Minimum Bachelor&rsquo;s Degree in Chemistry or related scientific discipline and minimum of 1 year experience in an analytical laboratory in pharmaceutical, biotech or other related industry required.</font></span></li> <li class="msonormal" style="margin-top:4px;"> <font face="Times New Roman" size="4"><span style="line-height: 115%;">Must possess working or practical </span><span style="line-height: 115%;">knowledge of laboratory testing of raw materials, in-process, finished products and/or stability samples such as dissolution, assay, content uniformity/blend uniformity, particle size distribution, density, water determination, and related testing in a FDA regulated laboratory environment.<o:p></o:p></span></font></li> <li class="msonormal" style="margin-top:4px;"> <span style="line-height: 115%;"><font face="Times New Roman" size="4">Must possess working or practical knowledge of the following:&nbsp; HPLC, UV, Dissolution, Karl Fisher (KF) and other analytical instrumentation.</font></span></li> <li class="msonormal" style="margin-top:4px;"> <span style="line-height: 115%;"><font face="Times New Roman" size="4">Must have basic understanding of cGMPs and compendia procedures where applicable (i.e., USP, NF, BP, etc.).<o:p></o:p></font></span></li> <li class="msonormal" style="margin-top:4px;"> <span style="line-height: 115%;"><font face="Times New Roman" size="4">Excellent written and oral communication skills required.</font></span></li> <li class="msonormal" style="margin-top:4px;"> <span style="line-height: 115%;"><font face="Times New Roman" size="4">Experience with Empower 3 or related lab software preferred.</font></span></li> <li class="msonormal" style="margin-top:4px;"> <span style="line-height: 115%;"><font face="Times New Roman" size="4">&nbsp;Proficient with Microsoft Office &nbsp;&ndash; Word and Excel required.</font></span></li> <li class="msonormal" style="margin-top:4px;"> <font face="Times New Roman" size="4"><span style="line-height: 115%;">Ability to effectively interact with others required. </span></font></li> <li class="msonormal"> <font face="Times New Roman" size="4">Must be able to lift 25 pounds to ensure that the person can carry out analytical testing in case of requirement.</font></li> <li class="msonormal"> <font face="Times New Roman" size="4">Ability and willingness to work overtime as required by business needs, including some nights and weekends.</font></li> </ul> </li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=726 http://pharmaboard.com/empid=726 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com QA Inspector <b>Experience:</b> 2 Year(s)<br/><b>Location:</b> New Jersey<br/><b>Industry Type:</b> Rx: Solid Dose / Tablets / Capsules<br/><b>Summary:</b> <p class="msonormal" style="background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;"> <span style="font-family:&quot;Cambria&quot;,&quot;serif&quot;;">Qualifications</span></p> <ul style="list-style-position: inside; margin-top: 0px; margin-left: 0px; padding-top: 0px; padding-left: 0px;"> <li class="msonormal" style="margin-left: 0px; text-indent: -18px; line-height: normal; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;"> <font size="3"><span style="font-family:&quot;Cambria&quot;,&quot;serif&quot;; ">High School Diploma or equivalent with a minimum 2 years of experience in a GMP environment required.</span></font></li> <li class="msonormal" style="margin-left: 0px; text-indent: -18px; line-height: normal; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;"> <font size="3"><span style="font-family:&quot;Cambria&quot;,&quot;serif&quot;; ">Experience in a pharmaceutical, biotech or related manufacturing environment preferred.</span></font></li> <li class="msonormal" style="margin-left: 0px; text-indent: -18px; line-height: normal; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;"> <font size="3"><span style="font-family:&quot;Cambria&quot;,&quot;serif&quot;; ">Experience working with various dosage manufacturing (solid, semi solid, liquid, etc) preferred.&nbsp; </span></font></li> <li class="msonormal" style="margin-left: 0px; text-indent: -18px; line-height: normal; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;"> <font size="3"><span style="font-family:&quot;Cambria&quot;,&quot;serif&quot;; ">Excellent attention to detail and strong record keeping skills required.</span></font></li> <li class="msonormal" style="margin-left: 0px; text-indent: -18px; line-height: normal; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;"> <font size="3"><span style="font-family:&quot;Cambria&quot;,&quot;serif&quot;; ">Excellent written and verbal communication required.</span></font></li> <li class="msonormal" style="margin-left: 0px; text-indent: -18px; line-height: normal; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;"> <font size="3"><span style="font-family:&quot;Cambria&quot;,&quot;serif&quot;; ">Basic Microsoft Office proficiency required; ERP experience preferred</span></font></li> <li class="msonormal" style="margin-left: 0px; text-indent: -18px; line-height: normal; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;"> <font size="3"><span style="font-family:&quot;Cambria&quot;,&quot;serif&quot;; ">Experience working under tight manufacturing deadlines required.&nbsp; </span></font></li> <li class="msonormal" style="margin-left: 0px; text-indent: -18px; line-height: normal; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;"> <font size="3"><span style="font-family:&quot;Cambria&quot;,&quot;serif&quot;; ">Excellent ability to identify and distinguish colors.<b> </b></span></font></li> <li class="msonormal" style="margin-left: 0px; text-indent: -18px; line-height: normal; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;"> <font size="3"><span style="font-family:&quot;Cambria&quot;,&quot;serif&quot;; ">Ability to lift up to 40 lbs required. </span></font></li> <li class="msonormal" style="margin-left: 0px; text-indent: -18px; line-height: normal; background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;"> <font size="3"><span style="font-family:&quot;Cambria&quot;,&quot;serif&quot;; ">Ability to work overtime and weekends as required.&nbsp; &nbsp;</span></font></li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=725 http://pharmaboard.com/empid=725 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Principal Scientist <b>Experience:</b> 8 Year(s)<br/><b>Location:</b> New Jersey<br/><b>Industry Type:</b> Rx: Liquids / Topicals / Powders / Softgel<br/><b>Summary:</b> <p class="msonormal" style="margin-bottom:0px;margin-bottom:0.00013333333333333334px;line-height: normal"> <b>Qualifications: </b></p> <p class="msonormal" style="margin-bottom:0px;margin-bottom:0.00013333333333333334px;line-height: normal"> <b>&nbsp;</b></p> <ul style="list-style-position: inside; margin-top: 0px; margin-left: 0px; padding-top: 0px; padding-left: 0px;"> <li class="msolistparagraphcxspfirst" style="margin-bottom:0px;margin-bottom:0.00013333333333333334px; text-indent:-18px;line-height:normal;"> <font size="3"><span>MS degree in Pharmaceutical Sciences/Pharmaceutics/Industrial Pharmacy or related science field from an accredited college or university with minimum of 10 years of related experience <b>OR</b> PhD in same with minimum of 8 years of related experience required.</span></font></li> <li class="msolistparagraphcxspmiddle" style="margin-bottom:0px;margin-bottom: 0.00013333333333333334px;text-indent:-18px;line-height:normal;"> <font size="3"><span>In-depth, hands-on experience in formulation for solid and liquid pharmaceutical dosage forms required. </span></font></li> <li class="msolistparagraphcxspmiddle" style="margin-bottom:0px;margin-bottom: 0.00013333333333333334px;text-indent:-18px;line-height:normal;"> <font size="3"><span>In-depth, working knowledge of novel drug delivery systems required.</span></font></li> <li class="msolistparagraphcxspmiddle" style="text-indent:-18px;"> <font size="3"><span style="line-height: 115%;">In-depth, hands-on exposure FDA, cGLP, cGMP, and SOP regulatory rules, regulations and guidelines required.</span></font></li> <li class="msolistparagraphcxspmiddle" style="text-indent:-18px;"> <font size="3"><span style="line-height: 115%;">Hands-on experience supervising, leading and training scientist and other laboratory personnel required.</span></font></li> <li class="msolistparagraphcxspmiddle" style="text-indent:-18px;"> <font size="3"><span style="line-height: 115%;">Advanced working knowledge of pharmaceutics, pharmaceutical sciences, and clinical pharmacokinetics required.</span></font></li> <li class="msolistparagraphcxspmiddle" style="text-indent:-18px;"> <font size="3"><span style="line-height: 115%;">In-depth, working knowledge of product formulation, products stability, packaging, and FDA submission methods and practices required.</span></font></li> </ul> <p class="msolistparagraphcxspmiddle"> <span style="line-height: 115%;">&nbsp;</span></p> <ul style="list-style-position: inside; margin-top: 0px; margin-left: 0px; padding-top: 0px; padding-left: 0px;"> <li class="msolistparagraphcxsplast" style="margin-bottom:0px;margin-bottom:0.00013333333333333334px; text-indent:-18px;line-height:normal;"> <font size="3"><span>Excellent verbal and written communication skills required.</span> <span>&nbsp;</span><span>Technical report writing experience required.</span></font></li> </ul> <p class="msonormal" style="margin-bottom:0px;margin-bottom:0.00013333333333333334px;line-height: normal"> <b>&nbsp;</b></p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=724 http://pharmaboard.com/empid=724 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Technical Writer <b>Experience:</b> 2 Year(s)<br/><b>Location:</b> New Jersey<br/><b>Industry Type:</b> Rx: Liquids / Topicals / Powders / Softgel<br/><b>Summary:</b> <ul> <li align="left" class="rtejustify1" style="margin-top:0px;margin-right:0px; margin-bottom:0px;margin-left:36px;margin-bottom:0.00013333333333333334px;text-align:left; text-indent:-18px;line-height:normal;"> <font size="3">Qualified candidates will hold a bachelor&rsquo;s degree and have minimum of 2 years of technical writing experience (SOPs, CAPAs, Customer Complaints, Investigations, etc.) in the pharmaceutical or biotech industry is required.</font></li> <li align="left" class="rtejustify1" style="margin-top:0px;margin-right:0px; margin-bottom:0px;margin-left:36px;margin-bottom:0.00013333333333333334px;text-align:left; text-indent:-18px;line-height:normal;"> <font size="3"><span lang="EN">Familiarity and exposure to pharmaceutical manufacturing and production is required. </span></font></li> <li align="left" class="rtejustify1" style="margin-top:0px;margin-right:0px; margin-bottom:0px;margin-left:36px;margin-bottom:0.00013333333333333334px;text-align:left; text-indent:-18px;line-height:normal;"> <font size="3"><span lang="EN"><span>&nbsp;</span>Current working knowledge of cGMPs in the pharmaceutical industry required.</span></font></li> <li align="left" class="rtejustify1" style="margin-top:0px;margin-right:0px; margin-bottom:0px;margin-left:36px;margin-bottom:0.00013333333333333334px;text-align:left; text-indent:-18px;line-height:normal;"> <font size="3"><span lang="EN">Excellent written and oral communication required.</span></font></li> <li align="left" class="rtejustify1" style="margin-top:0px;margin-right:0px; margin-bottom:0px;margin-left:36px;margin-bottom:0.00013333333333333334px;text-align:left; text-indent:-18px;line-height:normal;"> <font size="3"><span lang="EN">Experience conducting Quality or Compliance training is preferred.<span>&nbsp; </span></span></font></li> <li align="left" class="rtejustify1" style="margin-top:0px;margin-right:0px; margin-bottom:0px;margin-left:36px;margin-bottom:0.00013333333333333334px;text-align:left; text-indent:-18px;line-height:normal;"> <font size="3"><span lang="EN">Ability and willingness to work additional hours as needed required.<span>&nbsp;&nbsp;</span></span></font></li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=723 http://pharmaboard.com/empid=723 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Packaging Supervisor <b>Experience:</b> 4 Year(s)<br/><b>Location:</b> New Jersey<br/><b>Industry Type:</b> Rx: Liquids / Topicals / Powders / Softgel<br/><b>Summary:</b> <p class="msonormal"> <b>Job Qualifications:</b></p> <ul style="list-style-position: inside; margin-top: 0px; margin-left: 0px; padding-top: 0px; padding-left: 0px;"> <li class="msolistparagraphcxspfirst" style="text-indent:-18px;"> <font size="3">High School degree or equivalent AND 10+ years of related work experience required OR Associates degree AND 6+ years of related work experience required OR Bachelors degree AND a 4+ years of related work experience required.<span>&nbsp; </span>Related work experience includes all aspects of the manufacturing process in a pharmaceutical or biotechnology environment</font></li> </ul> <ul style="list-style-position: inside; margin-top: 0px; margin-left: 0px; padding-top: 0px; padding-left: 0px;"> <li class="msolistparagraphcxspmiddle" style="text-indent:-18px;"> <font size="3">Detailed knowledge of good manufacturing systems and familiarity with regulatory and Standard Operating Procedures (SOP) is required.</font></li> </ul> <ul style="list-style-position: inside; margin-top: 0px; margin-left: 0px; padding-top: 0px; padding-left: 0px;"> <li class="msolistparagraphcxspmiddle" style="text-indent:-18px;"> <font size="3">Packaging line experience required.</font></li> <li class="msolistparagraphcxspmiddle" style="text-indent:-18px;"> <font size="3">Excellent attention to detail and strong record keeping skills required.</font></li> <li class="msolistparagraphcxspmiddle" style="text-indent:-18px;"> <font size="3">Excellent written and verbal communication required.</font></li> <li class="msolistparagraphcxsplast" style="text-indent:-18px;"> <font size="3">Experience working under tight manufacturing deadlines required.</font></li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=722 http://pharmaboard.com/empid=722 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com RA Specialist <b>Experience:</b> 3 Year(s)<br/><b>Location:</b> New Jersey<br/><b>Industry Type:</b> Rx: Liquids / Topicals / Powders / Softgel<br/><b>Summary:</b> <ul> <li class="msolistparagraphcxspfirst" style="text-indent:-18px;"> <font size="3"><span style="font-family: &quot;Times New Roman&quot;, serif;">Bachelors degree in a scientific or life sciences discipline required.<span>&nbsp; </span>Masters is a plus.<span>&nbsp; </span></span></font></li> <li class="msolistparagraphcxspmiddle" style="text-indent:-18px;"> <font size="3"><span lang="EN" style="font-family: &quot;Times New Roman&quot;, serif;">Minimum of three years pharmaceutical industry experience required.<span>&nbsp; </span></span></font></li> <li class="msolistparagraphcxspmiddle" style="text-indent:-18px;"> <font size="3"><span lang="EN" style="font-family: &quot;Times New Roman&quot;, serif;">Hands on Regulatory Affairs experience preparing, submitting and maintaining IND, NDA, ANDA and/or DMF submissions in eCTD format highly preferred.<span>&nbsp; </span></span></font></li> <li class="msolistparagraphcxspmiddle" style="text-indent:-18px;"> <font size="3"><span lang="EN" style="font-family: &quot;Times New Roman&quot;, serif;">Microsoft Office (Word and Excel) proficiency required. </span></font></li> <li class="msolistparagraphcxspmiddle" style="text-indent:-18px;"> <font size="3"><span lang="EN" style="font-family: &quot;Times New Roman&quot;, serif;">Hands-on CMC experience and a strong understanding of CMC requirements preferred.<span>&nbsp; </span></span></font></li> <li class="msolistparagraphcxspmiddle" style="text-indent:-18px;"> <font size="3"><span lang="EN" style="font-family: &quot;Times New Roman&quot;, serif;">Excellent verbal and written communication skills required.<span>&nbsp; </span></span></font></li> <li class="msolistparagraphcxsplast" style="text-indent:-18px;"> <font size="3"><span lang="EN" style="font-family: &quot;Times New Roman&quot;, serif;">Must be able to work within a team as well as independently and be able to multi-task required.<span>&nbsp;&nbsp;</span></span></font></li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=721 http://pharmaboard.com/empid=721 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Scientist, Analytical R&D <b>Experience:</b> 3 Year(s)<br/><b>Location:</b> New Jersey<br/><b>Industry Type:</b> Rx: Liquids / Topicals / Powders / Softgel<br/><b>Summary:</b> <ul style="list-style-position: inside; margin-top: 0px; margin-left: 0px; padding-top: 0px; padding-left: 0px;"> <li class="msolistparagraphcxspfirst" style="margin-bottom:8px;text-indent:-18px;"> <font size="3"><span style="font-family:&quot;Arial&quot;,&quot;sans-serif&quot;">achelor&rsquo;s Degree in scientific discipline with 3-5 years of experience in pharmaceutical industry or an MS degree with 0-2 years of experience in pharmaceutical industry or an equivalent combination of education and experience required. </span></font></li> </ul> <p class="msolistparagraphcxspmiddle" style="margin-bottom:8px;"> <span style="font-family:&quot;Arial&quot;,&quot;sans-serif&quot;">&nbsp;</span></p> <ul style="list-style-position: inside; margin-top: 0px; margin-left: 0px; padding-top: 0px; padding-left: 0px;"> <li class="msolistparagraphcxsplast" style="text-indent:-18px;"> <font size="3"><span style="font-family: Arial, sans-serif;">Working knowledge of UV, IR, HPLC, GC and dissolution instruments operation, methods and techniques required.</span></font></li> </ul> <ul style="list-style-position: inside; margin-top: 0px; margin-left: 0px; padding-top: 0px; padding-left: 0px;"> <li class="msolistparagraphcxspfirst" style="margin-bottom:8px;text-indent:-18px;"> <font size="3"><span style="font-family:&quot;Arial&quot;,&quot;sans-serif&quot;">Strong PC and Microsoft Office skills required.</span></font></li> </ul> <ul style="list-style-position: inside; margin-top: 0px; margin-left: 0px; padding-top: 0px; padding-left: 0px;"> <li class="msolistparagraphcxspmiddle" style="margin-bottom:8px;text-indent:-18px;"> <font size="3"><span style="font-family:&quot;Arial&quot;,&quot;sans-serif&quot;">Familiarity with a FDA, cGLP, cGMP, and SOP regulatory rules, regulations and<span>&nbsp; </span><span>&nbsp;</span>guidelines.</span></font></li> <li class="msolistparagraphcxspmiddle" style="margin-bottom:8px;text-indent:-18px;"> <font size="3"><span style="font-family:&quot;Arial&quot;,&quot;sans-serif&quot;">Excellent oral and written communication required</span></font></li> <li class="msolistparagraphcxspmiddle" style="margin-bottom:8px;text-indent:-18px;"> <font size="3"><span style="font-family: Arial, sans-serif;">Ability to handle multiple projects at once required.<span>&nbsp;&nbsp;</span></span></font></li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=720 http://pharmaboard.com/empid=720 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com B2B Business Development <b>Experience:</b> 5 Year(s)<br/><b>Location:</b> New Mexico<br/><b>Industry Type:</b> Rx: Solid Dose / Tablets / Capsules<br/><b>Summary:</b> <p> REQUIREMENTS;</p> <p> A BS / BA degree is preferred.</p> <p> Excellent English language and communication skills are required.</p> <p> MIN. 2 years of b2b business development / sales experience. Pharmaceutical experience is NOT required, but selling a service product is preferred. Retail store experience is NOT applicable.</p> <p> Candidate must live in commuting distance to ABQ.&nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=719 http://pharmaboard.com/empid=719 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com General Manager <b>Experience:</b> 0 Year(s)<br/><b>Location:</b> New Jersey<br/><b>Industry Type:</b> Rx: Sterile non-aseptic<br/><b>Summary:</b> <p> <strong>Qualifications:</strong></p> <ul> <li> Bachelor&#39;s Degree in Life Science or other technical discipline with 10-12+ years of applicable experience [or]</li> <li> A Masters/Advanced degree and 10+ years of experience</li> <li> Understanding and working knowledge of GMP compliance, USP 795, 797 and 800 knowledge and experience</li> <li> At least 7 years of experience in Quality Assurance Operations Management [and] 4 years in Operations, Research and Development.</li> <li> Knowledge and a comprehensive understanding of biological and/or pharmaceutical technologies (sterile, biological, liquid, ointments, devices, solids, caplets, suspensions, granulations, soft elastic capsules, gel caps, extended release products, coating solutions and/or active pharmaceutical ingredients.</li> <li> Strong knowledge and experience with automation systems and related container enclosures (vials, bottles, syringes and other systems).</li> <li> Possesses knowledge and skill set to operate within an environment that requires a high degree of urgency, strong analytical and problem-solving skills interpersonal skills, ability to manage multiple complex tasks simultaneously, and capable of performing as leaders, members, and individuals.</li> <li> Experience interfacing with regulatory authorities, specifically FDA, regarding cGMP compliance.</li> </ul><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=718 http://pharmaboard.com/empid=718 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com Sen. QA Specialist <b>Experience:</b> 5 Year(s)<br/><b>Location:</b> New Jersey<br/><b>Industry Type:</b> Rx: Sterile aseptic<br/><b>Summary:</b> <p> BS in Science or Engineering</p> <p> Sterile experience preferred</p> <p> 5-7 years progressive QA experience in GMP production operation is required.</p> <p> &nbsp;</p><br/> http://pharmaboard.com/index.php?do=view_jobs&job_id=717 http://pharmaboard.com/empid=717 1969-12-31MST17:33:38-25200 1969-12-31MST17:33:38-25200 bob@protechpharma.com