About the Role
LAPORTE needs a Senior Pharmaceutical Validation Engineer in Greater Calgary. Bring your 5+ years of validation experience to ensure compliance and lead key validation activities in the pharmaceutical industry.
In this role, you'll manage validation tasks, from drafting master documents to executing protocols and ensuring GMP compliance. Your expertise will support clients in quality assurance; you'll handle deviations and manage client relationships effectively. Ideal candidates have a solid background in pharmaceutical processes and a willingness to travel.
Key Responsibilities: • Draft Validation Master Plans and other key documents • Create and execute IQ/OQ/PQ protocols for equipment • Ensure compliance with Good Manufacturing Practices • Support QA teams in initiating change notices • Manage and maintain client relationships effectively
Requirements: • Bachelor’s or master’s in science or engineering • At least 5 years’ experience in pharmaceutical sett...
In this role, you'll manage validation tasks, from drafting master documents to executing protocols and ensuring GMP compliance. Your expertise will support clients in quality assurance; you'll handle deviations and manage client relationships effectively. Ideal candidates have a solid background in pharmaceutical processes and a willingness to travel.
Key Responsibilities: • Draft Validation Master Plans and other key documents • Create and execute IQ/OQ/PQ protocols for equipment • Ensure compliance with Good Manufacturing Practices • Support QA teams in initiating change notices • Manage and maintain client relationships effectively
Requirements: • Bachelor’s or master’s in science or engineering • At least 5 years’ experience in pharmaceutical sett...
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