Gxp Supplier Quality Manager

Roche Holding AG

Mississauga, Ontario, Canada
Base: $105,560.00 - $138,547.50; bonus/equity: not...
Not specified
7-10 years gmp manufacturing experience
Oversight of cdmos and clinical supply operations
Development and negotiation of quality agreements
Roche Holding AG is seeking a GxP Supplier Quality Manager in Mississauga, Ontario, to oversee quality compliance of external partners in the pharmaceutical supply chain. The ideal candidate will have extensive experience in GMP manufacturing and quality assurance within the biotech or pharmaceutical industry

Job Summary

  • The role provides quality and compliance oversight of external partners including CDMOs, CROs, and in-licensing partners to ensure cGMP adherence.
  • Candidates will serve as the primary Quality Point of Contact for managing the full lifecycle of GMP suppliers from site selection to decommissioning.
  • Roche fosters a culture of personal expression and genuine connections where every voice matters in delivering life-changing healthcare solutions.

Matching Summary

Match Score: 85

Roche Holding AG is seeking a GxP Supplier Quality Manager in Mississauga, Ontario, to oversee quality compliance of external partners in the pharmaceutical supply chain. The ideal candidate will have extensive experience in GMP manufacturing and quality assurance within the biotech or pharmaceutical industry.

Salary

Base: $105,560.00 - $138,547.50; Bonus/Equity: Not specified; Benefits: Relocation benefits not available

Skills & Requirements

Must-have

  • 7-10 years GMP Manufacturing experience
  • Oversight of CDMOs and clinical supply operations
  • Development and negotiation of Quality Agreements
  • cGMP compliance monitoring and audit management
  • Experience with API and Drug Product release

Nice-to-have

  • Biologics manufacturing experience
  • Cross-cultural influence and collaboration skills
  • Agile and innovation mindset
  • Self-managed working style
  • SAP disposition experience for IMPs

Key Requirements

  • B.S., M.Sc. or PhD in life sciences
  • 7-10 years experience in pharmaceutical GMP Quality
  • Sound knowledge of ISO standards and international regulations

Work Rights

Not specified

Tailored Resume

Cover Letter