Job Title

OverviewCSV Engineer role at PharmEng Technology on 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.LocationEdmonton, Alberta (onsite role)Client IndustryPharmaceutical ManufacturingAbout PharmEng TechnologyPharmEng 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.Key ResponsibilitiesDevelop 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 readinessQualificationsProven 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 EdmontonIf youre a validation professional looking for your next consulting opportunity, wed like to hear from you. #J-18808-Ljbffr