Senior Validation Engineer in Pharmaceuticals

Advance your career at LAPORTE as a Senior Validation Engineer in Greater Calgary. Focus on GMP compliance and validation for superior quality in the pharmaceutical sector. LAPORTE is looking for a knowledgeable Senior Pharmaceutical Validation Engineer.

You'll draft master validation documents, execute qualification protocols, and ensure compliance with GMP standards. This role involves supporting QA teams and managing client relationships, ensuring high-quality manufacturing processes throughout. Key Responsibilities: • Draft master validation documents like Validation Master Plans • Execute qualification protocols (IQ/OQ/PQ) for critical systems • Ensure GMP compliance during all validation activities • Support QA teams in managing change notices effectively • Manage client accounts while maintaining strong relationships Requirements: • Bachelor’s or master’s degree in science or engineering • 5+ years in pharmaceutical manufacturing or consulting • Deep knowledge of GMP standards and procedures • Familiarity with pharmaceutical manufacturing processes • Willingness to travel to different client sites Utilize your validation expertise to enhance quality standards with LAPORTE in Calgary. #J-18808-Ljbffr