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CGMP Manufacturing Supervisor - Rotating Shift
Job in
St. Louis, Saint Louis, St. Louis city, Missouri, 63105, USA
Listed on 2026-01-24
Listing for:
The businesses of Merck KGaA, Darmstadt, Germany
Full Time
position Listed on 2026-01-24
Job specializations:
-
Manufacturing / Production
Production Manager, Manufacturing Engineer, Pharmaceutical Manufacturing, Manufacturing Operations / Plant Manager
Job Description & How to Apply Below
Your Role:
At Millipore Sigma, the cGMP Manufacturing Supervisor – Rotating Shift at our 3300 South Second Ave / Cherokee site will manage production personnel in the manufacture of products and many support functions outside of manufacturing. Job duties include:
- 12 hour rotating Day (6:00am - 6:30pm)/ Night (6:00pm - 6:30am) shifts with a 20% shift differential
- Oversee the manufacturing of Active Pharmaceutical Ingredients (API’s) regulated by the Food and Drug Administration and other regulatory bodies.
- This position will have direct reporting structures for scientists engaged in supporting the manufacturing operations, production coordinator, and manufacturing training program.
- Provide guidance Monday – Friday for scientists engaged in production readiness, including batch record review, equipment procurement, material transfer, training oversight and employee scheduling.
- This position will oversee a manufacturing training team currently consisting of persons on rotating shifts (Day and Night Shift).
- This position will oversee a manufacturing coordination team consisting of persons working Monday-Friday. Team responsibility includes material transfers from warehouse, material returns, and material consumptions.
- The position’s primary purpose is to ensure goods receipts are performed in a timely manner after manufacturing campaigns are complete.
- Lead a team of production scientists and operators in the scale-up, technology transfer, and execution of cGMP manufacturing.
- Develop employees’ knowledge and skills to improve performance and expand abilities as well as to coordinate the group’s efforts to meet departmental, company, and customer objectives.
- Adhere to protocols consistent with, and established according to, current Good Manufacturing Practices.
- Collaborate cross‑functionally with Project Management, MSAT, Process & Analytical Development, Quality Control, Quality Assurance, Packaging, Materials Management, Engineering, and Maintenance.
- Interact with customers’ project management, technical and quality teams.
- Maintain departmental goals and objectives safely and in compliance with all applicable federal, state, and company regulations (OSHA, EPA, FDA, EMA, etc.).
- Manage capital for equipment and facility improvements, including balancing the departmental budget. A primary responsibility is creating purchasing Process Orders.
- Support departmental efforts toward Process Improvement and company goals.
- Revise and approve procedures, batch records, and other documentation to ensure compliance with cGMP guidelines.
- Ensure employees remain current with all department and site training requirements.
- Assist and/or lead root cause investigations and implement effective corrective and preventative actions related to manufacturing deviations.
- Provide leadership and support of safety initiatives within production operations to ensure compliance with OSHA requirements.
- Ensure tasks are performed in accordance with approved site procedures, batch records, and protocols.
- Bachelor’s Degree in Chemistry, Biology, Biochemistry, Chemical Engineering, or another life science discipline.
- 4+ years of manufacturing experience in a cGMP setting.
- 1+ years of Management, Supervisory, or Lead experience.
- 3+ years of Management, Supervisory, or Lead experience in a GxP environment.
- Customer‑interfacing audit experience.
- Knowledge of Six Sigma concepts/Lean Manufacturing or process improvement.
- Familiarity with large‑scale cGMP process equipment, tangential flow, and chromatography automation.
- Strong Microsoft Office experience for manufacturing/operating procedure writing, technical report generation, product tracking and trending data analysis, and Operational Excellence reports.
- Strong interpersonal and conflict‑resolution skills.
- Advanced written and verbal communication skills.
Pay Range for this position: $88,800 - $152,300 a year.
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job‑related factors.…
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