M

Moderna

Develops mRNA-based medicines for health

Quality Assurance Intern

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Internship · Summer 2027Laval, QC, Canada

About the Job

Requirements

  • Currently enrolled in a Bachelor's or Master's degree program in a science, engineering, pharmacy, quality, life-sciences, or related discipline.
  • Basic proficiency with Microsoft Office applications, including Word, Excel, PowerPoint, and Outlook.
  • Ability to work carefully with controlled records and follow written procedures in a regulated environment.
  • Ability to work on-site at the Moderna Laval facility for the duration of the internship program.
  • Ability to complete all required training assignments in a timely manner and perform assigned activities in accordance with approved standard operating procedures, work instructions, and safety requirements.
  • Ability to maintain GxP, data-integrity, confidentiality, and site-safety requirements while partnering with Quality, Manufacturing, Digital/IT, and other functions.

Responsibilities

  • Support document control and records-management activities, including scanning, filing, archiving, retrieval, reconciliation, and organization of GMP records in accordance with approved procedures and retention requirements.
  • Assist with training administration activities, including tracking assigned training, supporting training records and reports, and following up on routine training-compliance activities.
  • Support preparation, formatting, routing, and administrative maintenance of controlled documents such as SOPs, work instructions, forms, and training materials under the direction of Quality personnel.
  • Assist with periodic reviews of Quality documentation and trackers to help ensure records remain current, complete, accurate, and inspection ready.
  • Support routine review and organization of electronic and paper GMP documentation for completeness and adherence to Good Documentation Practices; escalate observations to the responsible Quality team member.
  • Help maintain Quality metrics, dashboards, trackers, action lists, and meeting materials used to monitor Quality-system and operational performance.
  • Participate in Quality meetings and governance forums as appropriate, including capturing actions, maintaining trackers, and supporting follow-up activities.
  • Support Quality and cross-functional teams with data gathering, document retrieval, and preparation of information for audits, inspections, self-inspections, and compliance walkthroughs.
  • Identify and communicate potential documentation or process gaps to the responsible Quality team member and support implementation of approved improvements.
  • Support continuous-improvement initiatives focused on documentation practices, records management, training administration, digital tools, and operational efficiency.
  • Contribute to special projects and other Quality Assurance activities as assigned.

Desired Qualifications

  • Strong attention to detail, organization, and commitment to accurate documentation.
  • Strong written and verbal communication skills in a collaborative team environment.
  • Demonstrated ability to manage multiple assignments, meet timelines, and ask questions when clarification is needed.
  • Interest in Quality Assurance, GMP manufacturing, Quality Systems, or the biopharmaceutical industry.
  • Comfort working with data, trackers, electronic systems, and process-improvement activities.
  • A proactive, curious, and collaborative mindset with a willingness to learn in a fast-paced environment.
  • French and English communication skills are an asset for the Laval site.

About the Company

Moderna

Develops mRNA-based medicines for health

Moderna develops medicines built on messenger RNA (mRNA). Its products use mRNA delivered into cells to instruct them to produce specific proteins that can prevent or treat disease, with vaccines being a primary example. In practice, a dose delivers engineered mRNA into the body, cells translate it into a target protein, and the immune system responds or the protein modulates biology to combat disease. Moderna differentiates itself through its focus on building a whole mRNA medicines platform and in-house capabilities for designing, manufacturing, and scaling mRNA therapies, including rapid development and large-scale production. Its goal is to create a new category of medicines based on mRNA that can improve how diseases are discovered, developed, and treated, ultimately improving patient outcomes.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cambridge, MA
Founded
2010

Recently Posted Jobs

Explore more opportunities at Moderna

See more jobs