Posted 6 days ago
The Senior Manager, Site Environment, Health & Safety Lead will lead Moderna’s EHS function at its Laval mRNA drug-substance manufacturing facility as it transitions to full operations. Responsibilities include developing EHS strategy and management systems, managing risk and regulatory compliance, strengthening site safety culture, overseeing emergency preparedness and training, and driving environmental stewardship and continuous improvement.
Posted 7 days ago
The Operational Excellence Intern supports continuous improvement and operational effectiveness across Moderna’s Canadian operations. Responsibilities include documenting and improving workflows, developing policies and procedures, assisting governance, compliance, continuity and risk initiatives, and coordinating cross-functional projects and reporting.
Posted a month ago
The Quality Assurance Intern supports Quality operations and Quality Systems at Moderna’s cGMP manufacturing facility in Laval, including controlled documentation, records management, training administration, and audit preparation. The role also supports compliance, metrics tracking, and continuous-improvement activities while working with Quality and cross-functional teams under established procedures.
Posted a month ago
The Supply Chain Planning Co-Op supports production scheduling, material and inventory planning, master-data quality, and performance monitoring at Moderna’s Laval manufacturing site. The role collaborates with cross-functional teams and contributes to planning process improvements and a defined project, with the opportunity to work in a regulated GMP manufacturing environment.
Posted a month ago
The Quality Assurance Co-Op supports Quality operations and Quality Systems at Moderna’s cGMP manufacturing facility in Laval, maintaining controlled documentation, records, training administration, and compliance tracking. The role also assists with audit and inspection readiness, metrics, and continuous-improvement work under the direction of Quality personnel.
Posted a month ago
The Specialist, Quality Assurance provides real-time quality oversight for GMP manufacturing at Moderna’s Laval site. Responsibilities include monitoring compliance, managing deviations and change controls, supporting batch review and product disposition, maintaining documentation and data integrity, and overseeing contamination control, environmental monitoring, and facility sanitation programs.
Posted a month ago
The Site Quality Head leads end-to-end quality oversight for Moderna’s Canadian manufacturing and commercial operations, including the Laval site and external manufacturing partners. The role ensures GMP-compliant, inspection-ready quality systems and represents Quality with health authorities, while leading the quality organization, regulatory compliance, continuous improvement, and cross-functional initiatives.
Posted 3 months ago
No summary available
Posted 5 months ago
This role leads the establishment and operational readiness of a world-class Quality Control organization at Moderna's manufacturing site in Laval, Quebec. The Associate Director will oversee analytical testing, microbiology, environmental monitoring, and compliance activities to ensure product quality and regulatory adherence in a cGMP biotechnology environment.
Posted 6 months ago
This role leads Moderna's R&D collaboration strategy in Canada, defining and executing partnership-driven innovation initiatives to strengthen the company's position in the national life sciences ecosystem. The lead will bridge Moderna's global R&D organization with Canadian scientific institutions, developing business cases, aligning stakeholders, and advancing partnership models to accelerate scientific discovery and biomanufacturing goals.
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