Night Shift cGMP API Manufacturing Supervisor

Millipore Corporation

St. Louis (MO)

On-site

USD 89,000 - 152,000

Full time

6 days ago
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Benefits offered by this job

Health insurance
PTO
Retirement contributions

Job summary

MilliporeSigma seeks a cGMP Manufacturing Supervisor for the night shift in St. Louis, MO. You will manage production personnel and oversee the manufacture of FDA-regulated APIs, ensuring compliance and coordination with cross-functional teams.

You will lead a team of scientists and operators, drive training, scheduling, and equipment transfers while upholding GMP protocols and safety standards.

Qualifications

  • Bachelor's degree in a life sciences or chemical engineering discipline is required.
  • 4+ years of manufacturing experience in a cGMP setting.
  • 1+ year of supervisory/lead experience is required.

Responsibilities

  • Lead 12-hour night shifts (7:00pm–7:30am) with a 20% shift differential.
  • Oversee FDA-regulated API manufacturing and related operations.
  • Guide scientists and production staff in batch records, equipment, and scheduling.
  • Improve processes and ensure cGMP compliance across departments and facilities.

Skills

Leadership
Communication
Problem-solving
Safety awareness

Education

Bachelor's degree in Chemistry/Biology/Biochemistry/Chemical Engineering or Life Sciences

Tools

Microsoft Excel

Job description

MilliporeSigma seeks a cGMP Manufacturing Supervisor for the night shift in St. Louis, MO. You will manage production personnel and oversee the manufacture of FDA-regulated APIs, ensuring compliance and coordination with cross-functional teams.

You will lead a team of scientists and operators, drive training, scheduling, and equipment transfers while upholding GMP protocols and safety standards.

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