Group Manager - Quality Control

Pfizer Venezuela S.A

Unknown, Unknown, Venezuela
**
10+ years pharmaceutical industry experience
Cgmp compliance for quality control laboratories
Stability sample management and protocol approval
** Pfizer Venezuela S.A. is seeking a Group Manager for Quality Control, responsible for leading and managing QC teams, overseeing laboratory operations, and ensuring compliance with cGMP standards. The ideal candidate should have over 10 years of experience in the pharmaceutical industry, particularly in quality control, with strong leadership and technical skills. **

Job Summary

  • This role leads, coaches, and manages Quality Control teams through goal setting, performance reviews, and fostering a culture of accountability.
  • The position requires extensive knowledge of cGMP compliance including analytical testing, stability management, and equipment qualification lifecycle activities.
  • Candidates must demonstrate the ability to represent the department during internal, external, customer, and regulatory audits while ensuring data integrity.

Matching Summary

Match Score: 75

** Pfizer Venezuela S.A. is seeking a Group Manager for Quality Control, responsible for leading and managing QC teams, overseeing laboratory operations, and ensuring compliance with cGMP standards. The ideal candidate should have over 10 years of experience in the pharmaceutical industry, particularly in quality control, with strong leadership and technical skills. **

Skills & Requirements

Must-have

  • 10+ years pharmaceutical industry experience
  • cGMP compliance for Quality Control laboratories
  • Stability sample management and protocol approval
  • Equipment qualification IQ OQ PQ activities
  • Data integrity ALCOA+ principles
  • Audit handling and regulatory inspections
  • People leadership and performance management

Nice-to-have

  • Statistical tools and Six Sigma methodologies
  • Environmental testing and utility monitoring
  • Microbial identification and sterility testing
  • Generative AI tools like ChatGPT or Copilot
  • Method transfer from R&D to QC
  • Fostering teamwork and colleague development

Key Requirements

  • B. Pharm / M. Pharm / M.Sc. degree
  • Minimum 10+ years pharmaceutical industry experience
  • Extensive cGMP compliance knowledge
  • Proficiency in analytical techniques and QC instrumentation

Work Rights

Not specified

Tailored Resume

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