Pharmaceutical Validation Specialist

Elevate your career with LAPORTE as a Pharmaceutical Validation Specialist in Burnaby, BC. Leverage your validation expertise in a hybrid work environment while supporting operational compliance and client management.

LAPORTE, a premier consulting engineering firm, seeks a Senior Engineer and Specialist for its Greater Vancouver team. You will draft key validation documents, execute qualifications, and ensure compliance with Good Manufacturing Practices (GMP). Your experience will directly support clients' quality assurance and trigger essential corrective actions when needed.

Key Responsibilities:

• Draft essential validation documents including VMP and URS

• Execute equipment/system qualification protocols (IQ/OQ/PQ)

• Ensure compliance with GMP throughout validation processes

• Support change management and QA teams at client sites

• Manage and grow client accounts with excellence

Requirements:

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

• 5+ years’ experience in pharmaceutical validation

• In-depth knowledge of GMP standards

• Understanding of manufacturing processes in pharma

• Willingness to travel to client locations

Bring your validation mastery to LAPORTE and make an impact in pharmaceutical engineering.
#J-18808-Ljbffr