Group Manager - Quality Assurance

Pfizer

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10+ years experience in sterile dosage manufacturing
Strong knowledge of cgmp regulations
Experience with corporate quality systems
** Pfizer is seeking a Group Manager for Quality Assurance to oversee Batch Release activities, ensuring compliance with cGMP standards and effectively managing the workflow of the QA Batch Release department. The ideal candidate will have substantial experience in pharmaceutical quality assurance, strong leadership skills, and the ability to collaborate across departments. **

Job Summary

  • This role is primarily responsible for managing the daily activities of the QA Batch Release unit to ensure commercial batches are released to market compliantly.
  • The successful candidate will lead oversight for batch release activities, ensuring strict adherence to cGMP systems and procedures while collaborating with cross-functional departments.
  • Candidates must demonstrate strong leadership by developing succession plans, setting team goals, and implementing cost-saving initiatives within the Quality Assurance function.

Matching Summary

Match Score: 75

** Pfizer is seeking a Group Manager for Quality Assurance to oversee Batch Release activities, ensuring compliance with cGMP standards and effectively managing the workflow of the QA Batch Release department. The ideal candidate will have substantial experience in pharmaceutical quality assurance, strong leadership skills, and the ability to collaborate across departments. **

Skills & Requirements

Must-have

  • 10+ years experience in sterile dosage manufacturing
  • Strong knowledge of cGMP regulations
  • Experience with corporate quality systems
  • Proven people management and coaching skills
  • Ability to lead batch release approval processes

Nice-to-have

  • Master's degree in sciences or pharmacy
  • Experience interfacing with regulatory agencies
  • Proficiency in AI tools like ChatGPT or Copilot
  • Track record of driving continuous improvement
  • Strong analytical and problem-solving capabilities

Key Requirements

  • B. Pharm/M. Pharm / M.Sc. in Sciences
  • 10+ years experience in Manufacturing Quality or QA
  • Sterile dosage facility experience preferred
  • Not specified

Work Rights

Not specified

Tailored Resume

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