Associé(e) à la fabrication / Manufacturing Associate

Operate production equipment and prepare buffer solutions according to GMP standards and established SOPs.,Execute transcription, filtration, and purification processes using automated and computer-controlled systems.,Perform sampling and environmental control checks at critical process stages.,Apply performance tools and contribute to meeting operational KPIs.,Perform cleaning and sanitation of equipment and production/preparation areas.,Identify and report compliance and health/safety issues proactively to the supervisor.,Conduct routine maintenance tasks (lubrication, mechanical checks, filter changes).,Support continuous improvement initiatives and participate in projects across production.,Partner with QA to finalize documentation for batch release.,Participate in root cause analysis (RCA) and CAPA actions related to quality deviations or HSE incidents.,Act as a deputy for fellow Production Technicians or Supervisors in their absence.

3 to 5 years of experience in a GMP manufacturing environment.,Post-secondary degree in pharmaceutical sciences or biotechnology sector.,Ability to collaborate with peers, supervisors, and support function teams.,Excellent written and oral communication skills and excellent organizational skills.,Ability to pay attention to details while performing multiple tasks with minimal supervision.,Demonstrated commitment to Moderna's values (Bold, Collaboration, Curiosity and Relentless) and embody these values in the workplace.,Demonstrated aptitude or ability to learn to gain a strong understanding of GMP regulations.

Post-secondary degree in pharmaceutical sciences or biotechnology sector

Minimum of 2 years of work authorization required.,Pre-hire and periodic medical evaluations are required.,Moderna is a smoke-free, alcohol-free, and drug-free work environment.