CSV Engineer

Location : Edmonton, Alberta (onsite role)

Client Industry : Pharmaceutical Manufacturing

PharmEng Technology is seeking an experienced Computer 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 in IT Qualification and CSV within GMP-regulated environments

Strong documentation and validation protocol development skills

Effective communication and stakeholder coordination capabilities

Ability to work full-time on-site in Edmonton

About PharmEng Technology :

PharmEng Technology is a full-service consulting firm providing expert compliance and validation services to the pharmaceutical, biotechnology, and medical device industries. We pride ourselves on delivering high-quality solutions through industry expertise and collaborative client partnerships.

If you're a validation professional looking for your next consulting opportunity, we'd like to hear from you.

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