Found Description
Elevate your career as a Validation Engineer at AbCellera, where you will focus on compliance and quality assurance activities in our GMP setting. Your expertise in CQV will be pivotal in maintaining standards. Key Responsibilities
Manage CQV deliverables and documentation on electronic systems Lead investigations and provide solutions for compliance issues Facilitate internal and external audit processes Coordinate quality change controls effectively Conduct periodic system reviews for compliance Requirements
Bachelor's degree in Engineering, Chemistry, or a life science field At least 3 years of relevant experience Proficient with VLMS and QMS systems Detail-focused with solid organizational capabilities Ability to prioritize tasks in a fast‑paced environment
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Manage CQV deliverables and documentation on electronic systems Lead investigations and provide solutions for compliance issues Facilitate internal and external audit processes Coordinate quality change controls effectively Conduct periodic system reviews for compliance Requirements
Bachelor's degree in Engineering, Chemistry, or a life science field At least 3 years of relevant experience Proficient with VLMS and QMS systems Detail-focused with solid organizational capabilities Ability to prioritize tasks in a fast‑paced environment
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