CQV Focused Validation Engineer

Position: CQV Focused Validation Engineer Role
Join AbCellera as a Validation Engineer, where you will ensure compliance and quality assurance in our GMP setting. Your proficiency in CQV will play a critical role in maintaining operational standards.

This position centers on managing CQV deliverables, particularly on electronic systems. You will investigate compliance issues, propose practical solutions, and support internal and external audit processes. Effective coordination of quality change controls and regular compliance reviews are also critical aspects of this role.

Key Responsibilities:

• Manage CQV deliverables and documentation on electronic systems

• Lead investigations into compliance challenges

• Facilitate internal and external audits

• Coordinate quality change controls effectively

• Conduct periodic compliance reviews

Requirements:

• Bachelor's degree in Engineering, Chemistry, or related fields

• At least 3 years of relevant industry experience

• Familiarity with VLMS and QMS systems

• Strong attention to detail and organizational skills

• Ability to prioritize in a high-demand environment

Join AbCellera in driving quality assurance and compliance excellence in the life sciences sector.
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