(Fixed Term) Specialist, Quality Control
On-site · Laval, Quebec, Canada
Job Summary
Quality Control Analyst specializing in Microbiology & Bioassay at Moderna's Laval manufacturing facility. Role includes executing GMP QC Molecular Biology methods (molecular analytics, protein analytics, ELISA, cell-based potency), performing GMP QC Microbiology methods (sterility, bioburden, endotoxin), supporting testing for drug substances/products, conducting TOC/conductivity/bioburden/sterility/endotoxin analyses, participating in method transfers, audits, and equipment/method qualifications. Requires on-site presence, 2+ years work authorization, and a BSc/BA with 5 years of QC experience in a cGMP setting; fluency in French and English preferred. Close collaboration in a dynamic cross-functional environment with adherence to FDA/EU/ICH guidelines; role emphasizes investigations, project prioritization, and contributing to GMP laboratory operations.
Required Qualifications
- BSc/BA in a relevant scientific discipline with 5 years Quality Control experience in a cGMP organization with a focus in Molecular Biology, DNA Sequencing and Microbiology
- On-site full-time at Moderna site in Laval, Canada; not eligible for remote work
- Minimum 2 years work authorization required
- Pre-hire and periodic medical evaluations required for Health Canada compliance
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