INTERNSHIP DETAILS

2026 Intern - Quality Management

CompanyRoche
LocationMississauga
Work ModeOn Site
PostedJanuary 23, 2026
Internship Information
Core Responsibilities
The Quality Management Intern supports the QM team in ensuring compliance with regulatory requirements for product release and documentation management. They assist in monitoring group communications and maintaining necessary licenses.
Internship Type
full time
Salary Range
CA$57,416 - CA$75,358
Company Size
103600
Visa Sponsorship
No
Language
English
Working Hours
35 hours
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About The Company
Roche is a global pioneer in pharmaceuticals and diagnostics focused on advancing science to improve people’s lives. The combined strengths of pharmaceuticals and diagnostics under one roof have made Roche the leader in personalised healthcare – a strategy that aims to fit the right treatment to each patient in the best way possible. Roche is the world’s largest biotech company, with truly differentiated medicines in oncology, immunology, infectious diseases, ophthalmology and diseases of the central nervous system. Roche is also the world leader in in vitro diagnostics and tissue-based cancer diagnostics, and a frontrunner in diabetes management. Founded in 1896, Roche continues to search for better ways to prevent, diagnose and treat diseases and make a sustainable contribution to society. The company also aims to improve patient access to medical innovations by working with all relevant stakeholders. Thirty medicines developed by Roche are included in the World Health Organization Model Lists of Essential Medicines, among them life-saving antibiotics, antimalarials and cancer medicines. Roche has been recognised as the Group Leader in sustainability within the Pharmaceuticals, Biotechnology & Life Sciences Industry ten years in a row by the Dow Jones Sustainability Indices (DJSI). For more information, please visit https://careers.roche.com Read our community guidelines here: https://www.roche.com/some-guidelines.htm #Roche #Biotechnology #Pharmaceuticals #Diagnostics #Healthcare #PersonalisedHealthcare #GreatPlaceToWork #Innovation
About the Role
<p style="text-align:left">At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. </span></p><p><span>That’s what makes us Roche.</span></p><p><span>The Quality Management Intern works collaboratively with the Quality Management (QM) team, Health Canada, and Roche internal networks (local and global) to support compliance of processes and products to Pharma Quality System (PQS) and Health Canada requirements. Responsibilities may include management of documents, reviewing documents, supporting batch release, supporting licensing activities, liaising with other teams and supporting quality projects. QM Intern may also undertake other ad-hoc work or projects.</span></p><p><span>QM Intern will gain knowledge and understanding of Canadian Regulations, Good Manufacturing Practices (GMP and Medical Device) regulations to support quality compliance activities of Roche Canada.</span></p><p></p><p><b><b>The Opportunity:</b></b></p><ul><li><p><span>You are supporting the  QM team to obtain and review all required documentation for releasing products (commercial and clinical products) to the Canadian market ensuring compliance with regulatory requirements</span></p></li><li><p><span>You are helping to monitor group email accounts as this is essential in ensuring the work is well organized and executed.</span></p></li><li><p><span>You are learning and understanding global PQS directives and Health Canada GMP requirements to help ensure the activities you are supporting meet their expectations</span></p></li><li><p><span>You are assisting in the maintaining of both our Drug Establishment License and our Medical Device Establishment License.</span></p></li><li><p><span>You are learning and supporting the team with  change control and deviation processes as required</span></p></li><li><p><span>You are supporting the team by learning about critical processes and helping maintain required documentation ensuring they are consistently meeting both Health Canada and Roche requirements.</span></p></li></ul><p></p><p><b><b>Who you are:</b></b></p><ul><li><p><span>You hold a Bachelor's Degree in science.</span></p></li><li><p><span>You are currently pursuing a post-graduate certificate in Quality Assurance and Regulatory Affairs (e.g., Seneca, Humber, or an equivalent accredited program).</span></p></li><li><p><span>You have a general understanding of Health Canada regulations and guidelines</span></p></li><li><p><span>You have strong communication, problem solving, time management and  interpersonal skills</span></p></li><li><p><span>You have a  “We” over “Me” mentality, characterized by transparency and a desire to support team members whenever needed</span></p></li><li><p><span>You possess the ability to adopt agile mindsets and behaviors and integrate them into your daily tasks.</span></p></li><li><p><span>You have the ability to work efficiently and collaboratively within a high-performing team environment and be an integral member of a self-managing team.</span></p></li></ul><p></p><p><b><b>Additional Information:</b></b></p><ul><li><p><b><u>Term</u><u>:</u><span> </span></b><span>12-month full-time work term (35 hours per week).</span></p></li><li><p><b><u>Structure</u><u>:</u><span> </span></b><span>Hybrid work model (Majority of days in the office)</span></p></li><li><p><b><u>Timeline:</u><span> </span></b><span>Position begins in May 2026.</span></p></li></ul><p></p><p><b><b>Relocation benefits are not available for this posting. </b></b></p><p><span>#RocheInternshipCA2026</span></p><p></p>The expected salary range for this position based on the primary location of Mississauga is 57 416,00 and 75 358,50 of hiring range. Actual pay will be determined based on experience, qualifications, and other job-related factors as determined by the company.<p></p><p>We use artificial intelligence to screen, assess or select applicants for this role.</p><p></p><p>This posting is for an existing vacancy at Hoffmann-La Roche Ltd.</p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><div><div><div><div><div><div><div><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p></div></div></div></div></div></div></div>
Key Skills
CommunicationProblem SolvingTime ManagementInterpersonal SkillsTeamworkAgilityQuality AssuranceRegulatory AffairsGood Manufacturing PracticesHealth Canada RegulationsDocumentation ManagementBatch Release SupportLicensing ActivitiesChange ControlDeviation ProcessesQuality Compliance
Categories
HealthcareScience & Research