Validation Engineer
AbCellera • Vancouver, BC1d • $73,000 - $87,000
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Validation Engineer
AbCellera•Vancouver, BC
•$73,000 - $87,000
About The Position
Each of us cares about someone who will need medicines. That’s why our vision is to repeatedly beat the odds to deliver breakthrough medicines to patients that need them. We pursue truth and scientific rigour and have the courage to work at the edge of the unknown. We are looking for a Compliance/Validation Engineer to join the Engineering Asset Management team and support execution of CQV (Commissioning, Qualification, Validation) and engineering compliance activities, in alignment with regulatory expectations and Good Manufacturing Practices. This role is for you if you bring hands-on experience in a pharmaceutical or biotech environment, paired with sharp analytical thinking, a keen eye for detail, and the confidence to influence and align cross-functional teams.
Requirements
- Bachelor's degree in Engineering, Chemistry, or a related life science field
- 3+ years of experience in a similar role in a pharmaceutical or biotech environment
- Comfortable navigating electronic VLMS and QMS platforms
- Detail-oriented with strong documentation and organizational skills
- Proactive, can-do attitude to problem-solving
- Ability to thrive in a collaborative team setting and communicate clearly across functions
- Ability to juggle competing priorities and manage multiple tasks without letting anything slip through the cracks
Nice To Haves
- Familiarity with AutoCAD or Revit
Responsibilities
- Authoring and reviewing CQV protocols, SOPs, and technical documentation, ensuring everything meets rigorous GMP standards and holds up under scrutiny
- Leading investigations into deviations and non-conformances, driving CAPA implementation that gets to the root cause and keeps issues from coming back
- Being a trusted voice for the engineering team during internal and external audits
- Coordinating and executing engineering and quality change controls, keeping projects moving without compromising compliance
- Drafting and executing CQV deliverables, from User Requirement Specifications to protocols, summary reports, and periodic reviews, on an electronic VLMS
- Managing the full lifecycle of engineering drawings and documents through e-systems, bringing structure and precision to everything you touch
- Performing periodic reviews of all qualified systems at our GMP manufacturing facility to ensure ongoing compliance and performance
- Shaping how the team measures success by supporting the development and tracking of departmental KPIs
Benefits
- Equity
- Annual bonus dependent on team and company performance
- 6% (non-match) RRSP contribution
- CAD $1,500 annual Active Lifestyle Allowance
- Annual vacation
- Professional development opportunities
- Comprehensive health benefits
- Scientific and technical mentorship
- Strong sense of community and connections across AbCellera through work, clubs, and socials
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
251-500 employees
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