Validation Engineer Pharmaceutical Projects

Position: Validation Engineer for Pharmaceutical Projects
Explore an enriching career as a Validation Engineer at LAPORTE in Burnaby, BC. Focus on pharmaceutical validation and compliance in a supportive and hybrid work environment.

LAPORTE, an esteemed engineering consulting firm, is looking for a Senior Engineer & Specialist to strengthen its team in Greater Vancouver. You will draft critical validation documents, execute qualification protocols, and ensure GMP compliance throughout all phases of project execution. Collaborating with clients’ QA teams will be key in managing necessary change controls and compliance actions.

Key Responsibilities:

• Draft master validation documents, including risk analysis

• Execute thorough qualifications (IQ/OQ/PQ) for systems

• Monitor and ensure compliance with GMP standards

• Facilitate client QA/Compliance changes and CAPA processes

• Manage ongoing client relationships effectively

Requirements:

• Degree in science or engineering (BSc/MSc)

• Minimum of 5 years’ experience in relevant sectors

• Comprehensive knowledge of GMP practices

• Familiarity with pharmaceutical manufacturing workflows

• Willing to travel for client engagements

Bring your validation expertise to LAPORTE and play a vital role in shaping pharmaceutical compliance.
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