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Validation Engineer - Pharmaceutical Manufacturing
Job in
Cranbrook / EK, BC, V1A, Canada
Listed on 2026-10-15
Listing for:
Placements24
Full Time
position Listed on 2026-10-15
Job specializations:
-
Engineering
Quality Engineering, Pharma Engineer -
Quality Assurance - QA/QC
Quality Engineering
Job Description & How to Apply Below
Key Responsibilities Develop and execute validation protocols (IQ, OQ, PQ) for manufacturing equipment, facilities, and utilities.
Write and review validation reports, ensuring accuracy, completeness, and compliance with regulatory expectations.
Collaborate with engineering, manufacturing, and quality assurance teams to ensure seamless validation activities.
Maintain the validation status of equipment and systems through revalidation and change control processes.
Troubleshoot and resolve validation-related issues, ensuring minimal impact on production schedules.
Requirements Bachelor's degree in Engineering (Mechanical, Electrical, Chemical) or a related technical field.
Minimum of 3 years of experience in validation engineering within the pharmaceutical or related regulated industries.
Thorough understanding of cGMP , validation principles, and regulatory guidelines (e.g., FDA, EMA).
Experience with qualification of manufacturing equipment, HVAC systems, purified water systems, and process equipment.
Strong technical writing skills and the ability to manage multiple validation projects effectively.
Benefits Competitive annual salary and comprehensive benefits package.
Opportunity to gain extensive experience in pharmaceutical validation.
Professional development and training opportunities.
A supportive team environment focused on quality and compliance.
Contribute to the production of essential medicines in Kimberley .
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