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Manufacturing Supervisor provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Manufacturing Supervisor will be responsible for the planning of daily manufacturing activities per the weekly production calendar. This person will be responsible for the completion of assignments needed to execute a dynamic production schedule within the clean room cGMP facility. The supervisor will work with Engineering, Materials Management, Quality Assurance and Validation to complete assignments in a fast-paced and dynamic environment. Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture. Responsibilities
• Coordinate the activities of a work team, which may consist of several Manufacturing Technicians. Train and develop junior staff on aseptic technique and filling machine operation
• Responsible for working with management on team performance management, including annual reviews, disciplinary actions, training status, employee development plans, and succession planning
• Responsible for escalating any non-conforming events to the appropriate cross-functional stake holder

• Must be able to function independently or in a larger, cross-functional group
• Plan, oversee and participate in projects as necessary based on the department needs
• Can operate, troubleshoot and maintain manufacturing equipment and see through the maintenance process using work orders
• Conduct a daily walkthrough of the manufacturing facility to ensure status signs, logbooks and batch records are documented appropriately
• Willingness to perform and train aseptic processing operations and has the ability to serve as the lead operator in these activities
• Ensure direct reports maintain 100% up to date on their training curricula
• Conduct, coordinate and document quality/safety incidents and investigations, corrective and preventive actions
• May establish and maintain systems to track department deliverables and trend performance against metrics
• Ensure the cleanroom is equipped with the necessary materials, tools and equipment necessary
• Order supplies and issue work orders as needed
• Maintain manufacturing records, comply with cGMP’s and internal quality system requirements
• Work with Engineering, Materials Management, Quality Assurance and Validation to complete assignments, and ensure ongoing continuous improvement
• Ability to become fluent in all functional areas, and provide leadership, in the absence of the department/shift manager
• Perform hazardous waste handling operations in accordance with AMRI procedures
• Perform waste container filling operations and applying identification markers and labels
• Handle movement of waste from generation point to central accumulation area

• Bachelor’s Degree in related field required
• 5+ years of experience in pharmaceutical manufacturing
• Comprehensive understanding of cGMP compliance and proficiency with Windows-based Microsoft Office applications
• Ability to pass sterile gowning qualification required
• Excellent communication skills
• Desire to work collaboratively with clients, vendors, and supporting departments
• Must be versatile with strong prioritization skills
• Ability to delegate tasks appropriately to a wide range of skilled technicians and function Preferred
• Former supervision skills strongly preferred
• Previous cleanroom or cGMP experience is highly desirable
• Fill/finish or aseptic technique training strongly preferred

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