Take on a pivotal Validation Engineer role at AbCellera and ensure rigorous compliance through effective CQV activities. Your hands-on experience in GMP environments will drive continuous operational improvements.
Working within the Engineering Asset Management team, this position focuses on executing validation and qualification activities aligned with regulatory standards. With at least three years of experience, you'll be responsible for authoring necessary technical documents, leading investigations for continuous improvement, and ensuring internal audits reflect high compliance levels. Your analytical acumen will be essential in guiding the team and managing engineering documents with precision.
Key Responsibilities:
• Author CQV protocols and technical documentation
• Drive investigations into non-conformances
• Act as a key resource during audits
• Coordinate engineering change controls seamlessly
• Execute lifecycle management of engineering documents
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