Moderna

Moderna

Responsable d’équipe, Production de vaccins à ARNm – Quart de nuit / Team Lead, mRNA Vaccines Production - Night Shift

Laval - Canada, CA · Senior · Full-time

Work authorization requiredDetected 128 days ago
NLPSupply Chain5G/LTEGMPLeadershipCommunicationCollaborationOrganizational Skills

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odds of building a lasting career here

38Risky
Cap-exempt (no lottery)0
Sponsors this role85
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70

Thin sponsorship signal and lottery-bound. A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.

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Employer immigration record

from this employer's Department of Labor filings

Files H-1B transfers

1 transfer filing in the last year, covering 1 worker. Median labor-condition decision: 7 days. An employer that already files transfers is one that can take over an existing H-1B.

Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.

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About the role

  • Monitor team performance in accordance with key performance indicators in place and take necessary actions as needed.
  • 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.

Responsibilities

  • Participer à l'élaboration des dossiers de lots, des SOP et des supports de formation pour les processus opérationnels, cGMP ainsi que santé et sécurité.

Nice to have

  • Oversee the training, development, retention and performance of personnel for the execution of manufacturing operations.
  • Effectively communicate information relating to the production to management.
  • Work closely with QA peers to complete the necessary documentation for the release of commercial batches on time.
  • 5 to 10 years of experience in a GMP manufacturing environment.
  • 3 years of experience in personnel management
  • University degree in science/engineering.
  • 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.

Benefits

  • Ensure the application of cGMP, SOPs and health and safety rules in 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.

This listing is sourced directly from Moderna's careers page and normalized into a canonical job model.