(Fixed Term) Specialist, Quality Control

Moderna • Laval, QC

3d • Onsite

About The Position

Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. In Laval, Moderna’s long term partnership with the Government of Canada is strengthening the country’s pandemic preparedness. Our mRNA vaccine manufacturing facility will support rapid access to respiratory vaccines produced domestically. Through local talent development and research collaboration, we are building a strong mRNA ecosystem in Canada. Join us in shaping the future of biotechnology and healthcare innovation. At Moderna, this opportunity offers the chance to work at the forefront of mRNA technology within a highly collaborative GMP manufacturing environment focused on advancing global public health. As a Quality Control Analyst specializing in Microbiology & Bioassay, you will contribute directly to the analytical testing and operational excellence required to support critical vaccine manufacturing activities in Laval. Working within a rapidly evolving biotech landscape, you will perform advanced QC testing across molecular biology, microbiology, and bioassay platforms while supporting laboratory operations, method transfers, validations, and audit readiness. This role offers strong exposure to cutting-edge analytical technologies, digital laboratory environments, and opportunities to work closely with innovative scientific teams shaping the future of mRNA medicines and next-generation healthcare solutions.

Requirements

• 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.
• Hands on experience with molecular biology techniques including, but not limited to, gel electrophoresis, qPCR, and Sanger Sequencing.
• Hands-on experience of various Microbiology testing techniques and analyses (e.g. Vitek, Isolator Technology, Bioburden, BET, Sterility, others)
• Working experience in a GMP environment.
• Ability to collaborate effectively in a dynamic, cross-functional matrix environment.
• Ability to efficiently prioritize and complete multiple projects and tasks in a fast-paced environment.
• Proven ability to conduct investigations.
• Fluency in French and English as working language.

Nice To Haves

• Working knowledge of relevant and current FDA, EU, ICH guidelines and regulations preferred.
• A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.

Responsibilities

• Execute GMP Quality Control Molecular Biology methods with a focus on molecular and protein analytics
• Support ELISA and Cell-Based Potency testing activities within the QC laboratory
• Perform GMP QC Microbiology testing including Sterility testing, Bioburden Analysis, and Endotoxin testing
• Operate effectively within a GMP-regulated manufacturing and laboratory environment while maintaining compliance with quality standards and documentation practices
• Support analytical testing activities for both drug substance and drug product programs
• Generate analytical data to support studies and ongoing manufacturing activities as required
• Conduct Bioassay and Microbiology laboratory analysis including TOC, Conductivity, Bioburden, Sterility, and Endotoxin testing
• Contribute to efficient laboratory operations while supporting Moderna’s highly digital and innovation-driven quality systems environment
• Collaborate cross-functionally with Quality, Manufacturing, and external partners to ensure timely and compliant testing execution
• Participate in method transfer activities for both internal and external testing laboratories
• Support laboratory operational systems maintenance and continuous improvement initiatives
• Provide support during internal audits and vendor audits, ensuring inspection readiness and excellence
• Prepare and ship samples for contract laboratory testing activities
• Participate in equipment qualifications, method qualifications, validations, and analytical method transfers
• Contribute to Moderna’s mission of transforming medicine through advanced mRNA technologies and innovative laboratory science
• Gain exposure to emerging digital tools, automation, and advanced technologies that support the evolution of modern GMP laboratory operations and data-driven decision making

Benefits

• Best-in-class healthcare, plus voluntary benefit programs to support your unique needs
• A holistic approach to well-being with access to fitness, mindfulness, and mental health support
• Family building benefits, including fertility, adoption, and surrogacy support
• Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
• Savings and investments to help you plan for your future
• Location-specific perks and extras

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree