GMP QA Intern — Documentation & Records

Moderna Therapeutics; Laval (administrative region); On-site; CAD 51,000 - 59,000; Full time

Benefits offered by this job

On-site workspace

Job summary

Moderna Laval internships in Quality Assurance are full-time positions based in Laval, Canada from May to August 2027. The intern will support Quality operations and Quality Systems activities at Moderna’s cGMP facility, gaining exposure to GMP, controlled documentation, training administration, records management, and quality-system support in a regulated biopharma environment.

The role emphasizes documentation accuracy, inspection readiness, and collaboration with cross-functional teams, while

Qualifications

• 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 (Word, Excel, PowerPoint, Outlook).
• Ability to work on-site at the Moderna Laval facility for the duration of the internship.

Responsibilities

• Support document control and records-management activities (scanning, filing, archiving, retrieval).
• Assist with training administration (tracking training, records, reports).
• Maintain controlled documents (SOPs, work instructions, forms, training materials) under guidance.

Skills

Microsoft Office

On-site work

Education

Bachelor's or Master’s in science/engineering/pharmacy/quality/life sciences

Job description

Moderna Laval internships in Quality Assurance are full-time positions based in Laval, Canada from May to August 2027. The intern will support Quality operations and Quality Systems activities at Moderna’s cGMP facility, gaining exposure to GMP, controlled documentation, training administration, records management, and quality-system support in a regulated biopharma environment.

The role emphasizes documentation accuracy, inspection readiness, and collaboration with cross-functional teams, while