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Associé de fabrication-Quart de nuit​/Manufacturing Associate-Night Shift

Job in Laval, Province de Québec, Canada
Listing for: Moderna
Full Time position
Listed on 2026-01-16
Job specializations:
  • Manufacturing / Production
    Manufacturing Engineer
Job Description & How to Apply Below
Position: Associé de fabrication-Quart de nuit / Manufacturing Associate-Night Shift
The Role:

Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients' lives worldwide.

Moderna's long-term strategic partnership with the Canadian Government is revolutionizing the nation's pandemic preparedness and response capabilities. Our upcoming state-of-the-art mRNA vaccine manufacturing facility in Laval will play a pivotal role in ensuring rapid access to vaccines for respiratory viruses, contingent on Health Canada's approval. By investing in local talent development and fostering research and development collaborations, we are cementing Canada's position as a global center of mRNA excellence.

Join us as we build a resilient future in biotechnology and healthcare innovation.

This role involves operating production equipment in compliance with cGMP standards and health and safety regulations. The Technician will be responsible for key tasks across multiple stages of the manufacturing process, contributing to the production of mRNA vaccines. The successful candidate will need to demonstrate technical proficiency, a scientific mindset, and meticulous attention to detail in a fast-paced environment.

Here's What You'll Do:

Your key responsibilities will be:

  • Operating equipment and preparing buffer solutions for the manufacturing process.

  • Managing transcription, filtration, and purification processes using automated and computer-assisted equipment.

  • Sampling at critical stages of the process and conducting environmental controls.

  • Cleaning equipment and manufacturing/preparation areas.

  • Identifying and reporting compliance, health, and safety issues.

  • Performing routine maintenance tasks as required.

  • Collaborating with peers to achieve operational KPIs and continuous improvement initiatives.

Your responsibilities will also include:

  • Applying performance tools to support the team in meeting operational goals.

  • Contributing to multiple projects, enhancing efficiency in a dynamic, rapidly evolving environment.

  • Ensuring consistent compliance with cGMP standards and health and safety protocols throughout the manufacturing process.

The key Moderna Mindsets you’ll need to succeed in the role:

  • We prioritize the platform
    :
    In this role, the ability to focus on the broader goal of platform development while managing daily operational tasks is critical to driving success in mRNA vaccine manufacturing.

  • We act with urgency
    :
    The production environment requires swift, decisive action, and you'll need to keep the pace in order to meet the high demands of our manufacturing timelines.

Here’s What You’ll Bring to the Table:

  • 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.

  • Fluency in French and English in working language.

  • 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 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 workplace safety and in compliance with Health Canada requirements, pre-hire and periodic medical evaluations are required for this role.

Rémunération et avantages sociaux

Chez Moderna, nous croyons que lorsque vous vous sentez au mieux de votre…

Position Requirements
10+ Years work experience
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