About the role#
The Quality Assurance Co-Op supports Quality operations and Quality Systems at the Moderna cGMP manufacturing facility in Laval, Canada. This full-time position offers practical experience with Good Manufacturing Practices (GMP), controlled documentation, training administration, and records management within a regulated biopharmaceutical environment. You will work alongside experienced Quality professionals and cross-functional partners to maintain accurate, inspection-ready documentation and support compliance activities.
What you'll do#
- Manage document control and records activities, including scanning, filing, archiving, and retrieval of GMP records.
- Assist with training administration, such as tracking requirements and supporting compliance reports.
- Prepare, format, and maintain controlled documents like SOPs, forms, and training materials.
- Conduct periodic reviews of Quality documentation and trackers to ensure records are current and accurate.
- Review electronic and paper GMP documentation for completeness and adherence to Good Documentation Practices.
- Maintain Quality metrics, dashboards, action lists, and meeting materials.
- Participate in Quality meetings and governance forums, including capturing actions and supporting follow-up.
- Support cross-functional teams with data gathering and document retrieval for audits and inspections.
- Identify and communicate potential process gaps and support continuous-improvement initiatives.
- Partner with Manufacturing, Digital/IT, and other functions on assigned projects.
- Complete all required training and contribute to special Quality Assurance projects.
What you'll need#
- Currently enrolled in a Bachelor’s or Master’s degree program in Biology, Chemistry, Computer Engineering, Electrical Engineering, Mechanical Engineering, Pharmaceutical Sciences, or a related discipline.
- Basic proficiency with Microsoft Office, including Word, Excel, PowerPoint, and Outlook.
- Ability to work carefully with controlled records and follow written procedures in a regulated environment.
- Strong attention to detail, organization, and a commitment to accurate documentation.
- Ability to manage multiple assignments and meet timelines.
- Comfort working with data, trackers, and electronic systems.
- Proactive, curious, and collaborative mindset.
- Strong written and verbal communication skills.
- French and English communication skills are an asset.
Location & details#
- This role is based on-site at the Moderna facility in Laval, Quebec.
- This is a full-time, paid co-op position.
- Candidates must be available for the duration of the program.
About Moderna
Moderna operates in the biotechnology research sector. Founded in 2010, the company focuses on the development of mRNA therapeutics and vaccines. It maintains headquarters in Cambridge, Massachusetts. The organization employs between 1,001 and 5,000 people and functions as a public company.
How to get in at Moderna
Securing an internship at Moderna requires speed because high-volume roles often fill quickly. Intern Insider sends an instant alert the moment a role matching your target is published anywhere, so you apply among the first. Early applicants get seen before the pile grows, which gives you a distinct advantage over those who wait for a job board refresh. You should also look for ways to connect with the team directly. Intern Insider surfaces the recruiters behind the company roles so you can reach out to ask about the position or a referral. Reaching out to a human being instead of relying on an automated system materially improves your response rates.
