Responsable d'équipe, Production de vaccins à ARNm – Quart de nuit Emplois

Description du poste

The Production Supervisor is responsible for managing production and its team, in accordance with cGMP standards as well as health and safety regulations. The position also requires hands-on involvement in manufacturing processes and a high interest in technological innovations in mRNA.

Responsabilités

Manage all production operations and his team
Monitor team performance in accordance with key performance indicators in place and take necessary actions as needed
Collaborate with Supply Chain for planning: schedules, inventories, capacity
Manage/participate in several projects (processes, continuous improvement, equipment)
Deputy in case of absence: Production Supervisor colleague, Drug Substance Production Lead
Oversee the training, development, retention and performance of personnel for the execution of manufacturing operations
Manage team performance (recognition and rewards, succession plan as well as non-performance) through periodic interviews
Develop operational plans to ensure the success of the direct team and good communication with other teams on the commercial platform
Effectively communicate information relating to the production to management
Ensure the application of cGMP, SOPs and health and safety rules in production areas
Participate in the development of batch records, SOPs and training materials, for operational, cGMP and health and safety processes
Work closely with QA peers to complete the necessary documentation for the release of commercial batches on time
Investigate and participate in the writing of quality deviations as well as health and safety incidents in collaboration with the support departments

Exigences

5 to 10 years of experience in a GMP manufacturing environment
3 years of experience in personnel management
University degree in science/engineering
Ability to collaborate fluidly with peers, supervisors and support departments
Excellent writing, oral communication and organizational skills are required
Demonstrated commitment to Moderna's values (Bold, Collaboration, Curiosity and Relentless) and embody these values in the workplace
Demonstrated aptitude or ability to learn in order to gain a strong understanding of GMP regulations
This position is site-based, requiring you to be at Moderna's site full-time. This position is not eligible for remote work
As part of Moderna's commitment to build a sustainable workforce, a minimum of 2 years of work authorization is required for this role
As part of Moderna's commitment to workplace safety and in compliance with Health Canada requirements, pre-hire and periodic medical evaluations are required for this role

Ce que nous offrons

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 the future
Location-specific perks and extras

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Responsable d'équipe, Production de vaccins à ARNm – Quart de nuit

Description du poste

Responsabilités

Exigences

Ce que nous offrons

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