Senior Engineer, Validation at LAPORTE

Join LAPORTE as a Senior Engineer specializing in Pharmaceutical Validation in Burnaby, BC. Engage in hybrid work while leading compliance activities and fostering client relationships.

At LAPORTE, a trusted name in engineering consulting, you'll be part of the Greater Vancouver team.

Your role focuses on drafting validation master plans and executing cleaning and process qualification protocols. You’ll ensure adherence to GMP and provide critical support for clients’ QA teams during compliance initiatives.

Key Responsibilities:

• Create and maintain Validation Master Plans and specifications

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

• Uphold GMP compliance during validation work

• Assist QA teams with change notices and CAPA procedures

• Manage client accounts effectively and build strong relations

Requirements:

• Bachelor’s or master’s degree in relevant fields

• At least 5 years in the pharmaceutical industry or consulting

• Strong understanding of GMP and manufacturing processes

• Capacity to travel to client sites as needed

• Proven expertise in pharmaceutical validation

Utilize your validation skills at LAPORTE, contributing to excellence in the pharmaceutical industry.
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