AbCelleraVerified Job Source

QC Microbiology Manager

Vancouver, BC
On-site
Posted Aug 5, 2026
1 position

$105,600–$132,000 / year

Opens an external site

Employment type: Full-time
Experience level: Lead · 10+ years
Minimum education: Bachelor’s degree
Posting language: English
Working hours: 40 hours per week

Job summary

The QC Microbiology Manager leads laboratory operations, contamination control programs, and microbiological testing strategies at a GMP manufacturing facility. This role provides technical mentorship, oversees external testing, and ensures all microbiological data and processes comply with regulatory standards.

Job details

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 QC Microbiology Manager to lead GMP QC-Micro laboratory operations at AbCellera’s biological Drug Substance (DS) clinical manufacturing facility in Vancouver, Canada and to support external Contract Manufacturing Organizations (CMOs), Contract Testing Labs (CTLs), and other external collaborators. This position is responsible for strategic ownership of the Contamination Control Program at the site in alignment with regulatory expectations and industry best practices. You will provide deep technical mentorship, and troubleshooting expertise across microbial methods, EM programs, utilities monitoring, and contamination investigations. How you might spend your days Serving as the QC Microbiology SME for key strategic decisions related to microbiology, including contamination control (CCS), microbiological method strategy, environmental monitoring (EMPQ), utilities monitoring, raw materials, facility readiness, and risk-based testing approaches Leading all Microbiology operations, including bioburden, endotoxin, microbial ID, growth promotion, EM sampling, water testing, and trending Coordinating the execution of Disinfectant Efficacy (DET) studies to support our GMP manufacturing facility cleaning program Overseeing external microbiological testing, including reviewing and approving methods and testing results for raw materials, in-process, intermediate, and final product testing (DS, DP) Providing technical SME oversight of GMP cell banking and in-process bulk adventitious agents (mycoplasma, viral, etc.) Troubleshooting microbiological assays, contamination events, and EM deviations, ensuring timely and compliant resolution Leading or approving investigations of microbiology-related deviations, OOS results, EM excursions Verifying internal/contractor/partner QC-Micro data packages (batch records, test results, validation reports) for accuracy and adherence to ALCOA++ data integrity standards 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 Interfacing with all auditors (internal and external) to ensure positive audit outcomes Collaborating with Analytical Development, Quality Assurance, Materials, and Manufacturing teammates to ensure smooth operational flow and timely release/testing Creating, editing, and adhering to Standards and Standard Operating Procedures (SOPs) We'd love to hear from you if You bring deep 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 10+ 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 a fast-paced environment, cross-functional coordination, and prioritization of operational needs What we offer AbCellera’s hiring range for this role is CAD $105,600 - $132,000 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.

What you’ll do

Requirements

Candidates must have at least 10 years of hands-on QC microbiology experience in a GMP environment and a Bachelor's degree in Microbiology or a related life sciences field. Strong leadership, troubleshooting, and communication skills are required to manage complex laboratory operations and cross-functional collaborations.