Senior QA Consultant – GMP Compliance & Audits

Cencora, Inc.

Canada

À distance

CAD 95 000 - 135 000

Plein temps

Il y a 4 jours
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Avantages offerts par ce poste

Comprehensive benefits
Training programs
Professional development
Mentorship opportunities

Résumé du poste

Cencora, Inc. in Canada seeks a Senior Quality Assurance Specialist (Consultant) to support GMP/GDP compliant activities across drug and medical product releases. You will manage DELs/MDELs, coordinate supplier audits, and lead deviation investigations and CAPA programs.

You will interact with clients, manage documentation, and contribute to QA policy development while traveling up to 20% as needed. A Bachelor’s degree in a pharma-related field and 5+ years QA experience are required.

Qualifications

  • Bachelor’s degree in pharmaceutical/healthcare required.
  • 5+ years in Quality Assurance roles.
  • Strong knowledge of GMP/GDP and data integrity.
  • Experience with vendor audits is an asset.

Responsabilités

  • Maintain DELs/MDELs for multiple clients.
  • Coordinate document reviews for GMP compliance and product release.
  • Lead deviation investigations and CAPA with trend analysis.
  • Support audits/inspections (internal, client, regulatory).
  • Develop and revise QA policies and procedures; assist QA management.

Connaissances

GMP knowledge
CAPA RCA
Deviation handling
Auditing
Regulatory affairs
Documentation control

Formation

Bachelor's degree in pharma/healthcare

Outils

eQMS
EMS
WMS
CRM
QMS
MS Office

Description du poste

Cencora, Inc. in Canada seeks a Senior Quality Assurance Specialist (Consultant) to support GMP/GDP compliant activities across drug and medical product releases. You will manage DELs/MDELs, coordinate supplier audits, and lead deviation investigations and CAPA programs.

You will interact with clients, manage documentation, and contribute to QA policy development while traveling up to 20% as needed. A Bachelor’s degree in a pharma-related field and 5+ years QA experience are required.

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