Associate Manager - Mqa

pfizer.de

Cgmp compliance monitoring
Batch report and equipment audit review
Process and procedure simplification
The MQ TS Downstream Associate Manager is responsible for primary contact of quality on the floor, particularly in the Terminal sterilization, Visual Inspection and Packing areas of production and monitor processes for compliance to cGMP standards

Job Summary

  • The MQ TS Downstream Associate Manager is responsible for primary contact of quality on the floor, particularly in the Terminal sterilization, Visual Inspection and Packing areas of production and monitor processes for compliance to cGMP standards.
  • The role involves ensuring operating state of cGMP compliance, reviewing batch reports and equipment audit trails, performing process checks, and reporting observations to senior leadership.
  • The position requires identifying gaps and involving in process and procedure simplification to reduce downtime and increase efficiency.

Matching Summary

The MQ TS Downstream Associate Manager is responsible for primary contact of quality on the floor, particularly in the Terminal sterilization, Visual Inspection and Packing areas of production and monitor processes for compliance to cGMP standards.

Skills & Requirements

Must-have

  • cGMP compliance monitoring
  • Batch report and equipment audit review
  • Process and procedure simplification
  • Equipment breakdown assessment
  • Acceptable Quality Level sampling
  • Troubleshooting manufacturing processes

Nice-to-have

  • Experience with regulatory compliance and documentation
  • Strong organizational skills and attention to detail
  • Ability to mentor colleagues
  • Handling regulatory and internal audits

Key Requirements

  • B. Pharm, M. Pharm, or MSc degree
  • 6-8 years experience in Manufacturing Quality Assurance or Production
  • Experience in pharmaceutical manufacturing facility

Work Rights

Not specified

Tailored Resume

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