Job Title

Location: Edmonton, Alberta (onsite role)Client Industry:Pharmaceutical ManufacturingPharmEng 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 standardsProvide hands-on, on-site support and coordination with cross-functional teamsMaintain documentation, manage deviations, and support audit readinessQualifications:Proven experience in IT Qualification and CSV within GMP-regulated environmentsStrong documentation and validation protocol development skillsEffective communication and stakeholder coordination capabilitiesAbility to work full-time on-site in EdmontonAbout 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. #J-18808-Ljbffr