Senior Quality Control Analyst

Reposted 2 Days Ago
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Vancouver, BC, CAN
In-Office
88K-110K Annually
Senior level
Biotech
The Role
Lead hands-on QC microbiology operations including bioburden, endotoxin, microbial ID, EM sampling, utilities monitoring, contamination investigations, and mentorship. Ensure GMP inspection readiness, oversee sample workflows, review microbiology documentation, and troubleshoot assays and deviations to maintain data integrity.
Summary Generated by Built In

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 highly skilled, hands-on Senior Quality Control Analyst to provide deep technical mentorship in the day-to-day QC laboratory operations, with a primary focus on Microbiology. You will provide a strong in-lab presence and lead troubleshooting expertise across microbial methods, EM programs, utilities monitoring, and contamination investigations.

How you might spend your days

  • Leading Microbiology operations, including bioburden, endotoxin, microbial ID, growth promotion, EM sampling, water testing, and trending
  • Troubleshooting microbiological assays, contamination events, and EM deviations, ensuring timely and compliant resolution
  • Providing daily in-lab mentorship to the QC team, fostering strong technique, aseptic practices, and microbiological best practices
  • Ensuring microbiology labs and adjacent QC spaces remain inspection-ready, including GMP housekeeping and equipment readiness
  • Coordinating stability pulls, sample preparation, testing, and data tracking across QC programs
  • Overseeing sample receipt, chain-of-custody, aliquoting, storage conditions, and distribution workflows
  • Supporting routine sampling, testing, and trending of Utilities (WFI, clean steam, compressed gases) with appropriate documentation
  • Reviewing micro data packages, protocols, reports, and testing documentation for accuracy and adherence to ALCOA++ principles

We'd love to hear from you if

  • You bring deep, hands-on Microbiology experience in a regulated (GMP) QC environment, and are confident in leading microbial methods, EM programs, utilities monitoring, and contamination troubleshooting
  • You have experience mentoring or leading team members working within microbiology labs or cleanroom/controlled environments
  • You have 8+ years of hands-on QC microbiology experience in a GMP setting, in addition to a Bachelor’s degree in Microbiology or a related life sciences field
  • You communicate clearly, collaborate well, and maintain calm, structured decision-making under pressure
  • You demonstrate strong ownership, accountability, and a solutions-focused mindset when supporting analysts or resolving micro-related issues
  • You are organized, detail-oriented, and committed to inspection readiness and data integrity
  • You thrive in an environment requiring in-lab leadership, cross-functional coordination, and prioritization of operational needs

What we offer

AbCellera’s hiring range for this role is CAD $88,000 to $110,000 annually, commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. 

You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

About AbCellera

Creating medicines is the most important work we can do.

We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline.

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply

Please submit your application through our website and refer to Job ID 23334 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

Top Skills

Alcoa++ (Data Integrity)
Aseptic Technique
Bioburden Testing
Chain-Of-Custody Workflows
Clean Steam
Compressed Gases Utilities Monitoring
Endotoxin (Lal) Testing
Environmental Monitoring (Em) Sampling And Programs
Growth Promotion Testing
Microbial Identification
Stability Sampling And Testing
Water For Injection (Wfi)
Water Testing
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The Company
HQ: Vancouver, British Columbia
600 Employees
Year Founded: 2012

What We Do

AbCellera is breaking the barriers of conventional antibody drug discovery to bring better medicines to patients, sooner. AbCellera’s engine integrates expert teams, technology, and facilities with the data science and automation needed to propel antibody-based medicines from target to clinic in nearly every therapeutic area with precision and speed. AbCellera provides innovative biotechs and leading pharmaceutical companies with a competitive advantage that empowers them to move quickly, reduce cost, and tackle the toughest problems in drug development.

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