GMP-Driven Pharma Production Supervisor (Ops Leader)

Pfizer Inc

McPherson (KS)

On-site

USD 83,000 - 138,000

Full time

6 days ago
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Benefits offered by this job

401(k) Matching Contributions
Paid vacation
Paid holidays

Job summary

Pfizer Inc. in the United States is seeking an Operations Supervisor to direct multi-shift activities in production areas, including API and Drug Product manufacturing, with responsibility for both manual and automated processes in aseptic environments.

You will lead a team, manage staffing, ensure GMP compliance, and collaborate with Quality and Maintenance to keep production on schedule while driving continuous improvement and safety on the manufacturing floor.

Qualifications

  • Bachelor's degree in Engineering, Business, or Science with 2+ years of leadership experience or equivalent
  • Ability to manage multiple priorities in a fast-paced environment
  • Working knowledge of SAP or equivalent inventory management software
  • Proficient with Microsoft Office (Outlook, Word, Excel, PowerPoint, Visio)

Responsibilities

  • Supervise colleague activities in production of APIs, biotechnology products, or Drug Products in GMP-compliant manner.
  • Engage in colleague development with timely performance feedback and IDPs.
  • Ensure training is maintained and compliant with procedures and standards.
  • Schedule staffing to meet forecasted production within budget.
  • Collaborate cross-functionally to maintain schedule with Quality, Maintenance, and Warehouse teams.
  • Lead continuous improvement initiatives to reduce waste and improve safety and product quality.

Skills

Leadership
Problem solving

Education

Bachelor's degree in Engineering, Business, or Science with 2+ years of leadership experience

Tools

SAP
Microsoft Office

Job description

Pfizer Inc. in the United States is seeking an Operations Supervisor to direct multi-shift activities in production areas, including API and Drug Product manufacturing, with responsibility for both manual and automated processes in aseptic environments.

You will lead a team, manage staffing, ensure GMP compliance, and collaborate with Quality and Maintenance to keep production on schedule while driving continuous improvement and safety on the manufacturing floor.

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