CSV Engineer
CSV Engineer
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Job Description
Location: Edmonton Alberta (onsite role)
Client Industry: Pharmaceutical Manufacturing
PharmEng Technology is seeking an experienced Computer System Validation (CSV) Specialist for a 12month onsite 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:
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Develop and execute validation protocols (URS FS IQ OQ)
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Qualify laboratory and manufacturing equipment (e.g. sterile filling lines HVAC HPLC)
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Perform CSV activities in compliance with cGMP and regulatory standards
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Provide handson onsite support and coordination with crossfunctional teams
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Maintain documentation manage deviations and support audit readiness
Qualifications:
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Proven experience in IT Qualification and CSV within GMPregulated environments
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Strong documentation and validation protocol development skills
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Effective communication and stakeholder coordination capabilities
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Ability to work fulltime onsite in Edmonton
About PharmEng Technology:
PharmEng Technology is a fullservice consulting firm providing expert compliance and validation services to the pharmaceutical biotechnology and medical device industries. We pride ourselves on delivering highquality solutions through industry expertise and collaborative client partnerships.
If youre a validation professional looking for your next consulting opportunity wed like to hear from you.
Employment Type
Full Time
