CQV Engineer for AbCellera

Join AbCellera as a Compliance/Validation Engineer, focusing on CQV activities and regulatory compliance in a GMP environment. Contribute to protocols, investigations, and audits to ensure company standards are met. As a Compliance/Validation Engineer, you'll become an essential part of our Engineering Asset Management team.

This role requires you to author and review protocol documents, lead investigations into non-conformances, and assist in internal and external audits. You will drive compliance while executing quality change controls and managing engineering documentation throughout its lifecycle. Key Responsibilities: • Author and review CQV protocols, SOPs, and documentation • Lead investigations into deviations and drive CAPA actions • Support during internal and external audits • Manage engineering change controls for compliance • Perform periodic reviews of manufacturing systems Requirements: • Bachelor's degree in Engineering, Chemistry, or related field • 3+ years experience in a similar role • Familiarity with electronic VLMS and QMS platforms • Detail-oriented with excellent organizational skills • Ability to manage multiple priorities effectively Be part of AbCellera’s success by enhancing compliance and engineering integrity through your expertise. #J-18808-Ljbffr