Senior Engineer in Pharmaceutical Validation

LAPORTE is searching for a Senior Engineer in Pharmaceutical Validation in Greater Calgary. Your 5+ years of expertise will be vital in managing validation processes and ensuring compliance with industry standards.

You will be instrumental in drafting master documents, executing validation protocols, and maintaining adherence to Good Manufacturing Practices. Supporting client QA teams and managing accounts will be part of your responsibilities. A background in pharmaceutical processes combined with a willingness to travel is essential.

Key Responsibilities:

• Write Validation Master Plans and other documents

• Execute qualification protocols for systems and processes

• Ensure compliance with GMP standards

• Provide QA support on change notices and deviations

• Manage relationships with client accounts

Requirements:

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

• Over 5 years of experience in pharmaceutical environments

• Strong knowledge of GMP compliance

• Understanding of pharmaceutical manufacturing

• Openness to travel to client sites

Enhance pharmaceutical validation efforts and ensure quality compliance as a Senior Engineer with LAPORTE in Calgary.
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