Moderna
Responsable d’équipe, Production de vaccins à ARNm – Quart de nuit / Team Lead, mRNA Vaccines Production - Night Shift
Laval - Canada, CA · Full-time
Sponsorship not specifiedDetected 15 days ago
ViteNLPSupply ChainInventory ManagementGMPLeadershipCommunicationCollaborationOrganizational Skills
About the role
- Joining Moderna means advancing mRNA science to transform medicine.
- We don't have to be the smartest, we have to learn the fastest.
- We digitize everywhere possible using the power of code to maximize our impact on patients.
Responsibilities
- Lead and manage all production operations and the associated manufacturing team.
- Maintain hands-on involvement in manufacturing processes while providing operational leadership.
- Partner closely with Supply Chain colleagues to support production planning activities, including scheduling, inventory management, and manufacturing capacity planning.
- Lead and participate in projects related to manufacturing processes, continuous improvement initiatives, and equipment implementation or optimization.
- Support operational excellence initiatives that improve efficiency, reliability, quality, and manufacturing performance.
- Serve as deputy during the absence of a Production Supervisor colleague or the Drug Substance Production Lead.
- Drive effective communication of production-related information, priorities, risks, and achievements to management.
- Lead, coach, develop, and retain a high-performing manufacturing team responsible for executing production operations.
- Develop operational plans that support team success while fostering strong collaboration across the broader commercial manufacturing platform.
- Oversee training and qualification activities to ensure personnel are prepared to perform manufacturing activities safely, effectively, and in compliance with regulatory requirements.
Requirements
- Monitor team performance against established key performance indicators and implement corrective or improvement actions when required.
- Manage employee performance through regular performance discussions, recognition and reward programs, succession planning, and performance improvement activities when required.
- Partner closely with Quality Assurance teams to ensure all required documentation is completed accurately and on time to support commercial batch release.
- 5 to 10 years of experience in a GMP manufacturing environment.
- 3 years of experience in personnel management.
- University degree in science/engineering.
- The position requires proficiency in both French and English due to interactions with teams, partners, and tools located outside Quebec.
- Excellent writing, oral communication and organizational skills are required.
- Demonstrated aptitude or ability to learn in order to gain a strong understanding of GMP regulations.
Nice to have
- Gérer l'ensemble des opérations de production ainsi que son équipe.
- Participer activement aux activités de fabrication tout en assurant la supervision des opérations quotidiennes.
- Suivre la performance de l'équipe conformément aux indicateurs clés de performance (KPI) en place et prendre les mesures nécessaires au besoin.
- Collaborer étroitement avec la chaîne d'approvisionnement (Supply Chain) pour la planification des calendriers de production, la gestion des stocks et l'optimisation des capacités manufacturières.
- Gérer ou participer à plusieurs projets liés aux processus, à l'amélioration continue et aux équipements.
- Contribuer à l'optimisation des procédés et à l'amélioration de la performance opérationnelle de la plateforme manufacturière.
- Communiquer efficacement aux équipes de direction les informations relatives à la production, aux priorités opérationnelles et aux résultats.
- Superviser la formation, le développement, la rétention et la performance du personnel responsable de l'exécution des opérations de fabrication.
Skills
- Se joindre à Moderna, c'est faire progresser la science de l'ARNm pour transformer la médecine.
Benefits
- Build an engaged team culture focused on accountability, continuous learning, operational excellence, and innovation.
- Ensure strict adherence to cGMP requirements, Standard Operating Procedures (SOPs), and health and safety regulations across production areas.
Visa & Work Authorization
- As part of Moderna's commitment to build a sustainable workforce, a minimum of 2 years of work authorization is required for this role.
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This listing is sourced directly from Moderna's careers page and normalized into a canonical job model.