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CSV Engineer - Jobs in Edmonton

Job LocationEdmonton
EducationNot Mentioned
SalaryNot Mentioned
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypeFull time

Job Description

Location: Edmonton, Alberta (onsite role) Client Industry: Pharmaceutical ManufacturingPharmEng 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 #39;re a validation professional looking for your next consulting opportunity, we #39;d like to hear from you.

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