Pharmaceutical Validation Specialist

Position: Pharmaceutical Validation Specialist Hybrid Role
Enhance your validation expertise as a Pharmaceutical Validation Specialist at LAPORTE in Burnaby, BC. Enjoy a hybrid work model while ensuring compliance and managing client relationships.

At LAPORTE, a prominent consulting engineering firm, you will play a crucial role within the Greater Vancouver team. Your responsibilities include drafting validation documents and executing qualifications to meet Good Manufacturing Practices (GMP). You will directly support the quality assurance processes for clients and initiate corrective actions when necessary.

Key Responsibilities:

• Prepare key validation documents such as VMP and URS

• Conduct equipment and system qualification protocols (IQ/OQ/PQ)

• Maintain compliance with GMP during validation workflows

• Assist client site change management and QA teams

• Manage and expand client accounts with excellence

Requirements:

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

• More than 5 years of experience in pharmaceutical validation

• Strong knowledge of GMP standards

• Insight into pharmaceutical manufacturing processes

• Readiness to travel to various client locations

Bring your validation skills back to LAPORTE and influence pharmaceutical engineering positively.
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