Job Description
Location: Edmonton, Alberta (onsite role)
Client Industry: Pharmaceutical Manufacturing
PharmEng Technology is seeking an experiencedComputer System Validation (CSV) Specialist for a 12-month on-site consulting engagement with our client in Edmonton, Alberta. This role is essential in supporting GMP compliance for critical laboratory systems and software in a sterile manufacturing environment.
Key Responsibilities:
Develop and execute validation protocols (URS, FS, IQ, OQ)
Qualify laboratory and manufacturing equipment (e.g., sterile filling lines, HVAC, HPLC)
Perform CSV activities in compliance with cGMP and regulatory standards
Provide hands-on, on-site support and coordination with cross-functional teams
Maintain documentation, manage deviations, and support audit readiness
Qualifications:
Proven experience i...
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