Senior Pharmaceutical Validation Engineer

Advance your career at LAPORTE as a Senior Pharmaceutical Validation Engineer, based in Burnaby, BC. Utilize your validation skills in a hybrid setting to ensure compliance and efficient client management.

LAPORTE, a top-tier consulting services firm, is in search of a specialized engineer to support its Greater Vancouver operations. You will draft critical validation documents and execute qualification protocols essential for adhering to Good Manufacturing Practices (GMP).

Your role will ensure clients receive top-quality assistance while implementing necessary corrective measures.

Key Responsibilities:

• Draft essential validation documents including VMP and URS

• Execute qualification protocols: IQ, OQ, PQ

• Ensure GMP compliance throughout all validation stages

• Support client site change management and QA teams

• Cultivate and manage client accounts effectively

Requirements:

• Bachelor’s or master’s degree in science or engineering

• 5+ years of pharmaceutical validation experience

• Deep understanding of GMP standards

• Familiarity with pharmaceutical manufacturing processes

• Willingness to travel for client engagements

Bring your expertise in validation and compliance to LAPORTE and drive excellence in pharmaceutical engineering.
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