Manager, Quality Operations

Bristol Myers Squibb UK

Boudry, Switzerland
On-site
Quality oversight of contract manufacturing organizations
Cmo disposition documentation and annual product review
Assure cmo compliance with cgmp and regulatory standards
Bristol Myers Squibb is seeking a Manager of Quality Operations in Boudry, Switzerland, responsible for overseeing quality assurance for Contract Manufacturing Organizations (CMOs). The role involves ensuring compliance with Good Manufacturing Practices (cGMP) and regulatory standards while supporting product disposition and quality metrics

Job Summary

  • This quality manager provides quality oversight of Contract Manufacturing Organizations (CMOs), supporting management of disposition documentation and Annual Product Review.
  • Responsibilities include performing product disposition activities, ensuring CMO compliance with cGMP and regulatory standards, and managing quality metrics related to CMO performance.
  • The role requires strong negotiation, communication, and problem-solving skills, with a minimum of four years of experience in pharmaceutical operations and at least two years in Quality.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Manager of Quality Operations in Boudry, Switzerland, responsible for overseeing quality assurance for Contract Manufacturing Organizations (CMOs). The role involves ensuring compliance with Good Manufacturing Practices (cGMP) and regulatory standards while supporting product disposition and quality metrics.

Skills & Requirements

Must-have

  • Quality oversight of Contract Manufacturing Organizations
  • CMO disposition documentation and Annual Product Review
  • Assure CMO compliance with cGMP and regulatory standards
  • Perform product disposition activities
  • Manage and report quality metrics for CMO performance
  • Support inspection readiness and filing submission readiness

Nice-to-have

  • Balance business implications and quality decisions
  • Negotiation and influencing without authority
  • Rapid adaptation to changing environments
  • Strategic and analytical thinking skills

Key Requirements

  • Minimum 4 years pharmaceutical operations experience
  • Minimum 2 years Quality experience
  • B.S. degree in relevant scientific discipline
  • Experience in aseptic, sterile, and biological drug product manufacturing
  • Experience in contract manufacturing or contract testing
  • Proficiency with global systems (e.g. SAP, Microsoft Office)

Work Rights

Not specified

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