About The Job 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 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 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 handson, onsite support and coordination with crossfunctional teams Maintain documentation, manage deviations, and support audit readiness Qualifications Proven experience in IT Qualification and CSV within GMPregulated environments Strong documentation and validation protocol development skills Effective communication and stakeholder coordination capabilities Ability to work fulltime onsite 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 highquality 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. #J-18808-Ljbffr
Job Title
CSV Engineer