About the role#
This co-op position supports the Quality and Regulatory Affairs team within a medical-device manufacturing environment. You will gain hands-on experience by working with the Manufacturing Engineering Quality Assurance team to maintain documentation, manage non-conformance processes, and contribute to continuous improvement projects.
What you'll do#
- Support the review, approval routing, and revision control of quality system documents.
- Maintain records in the electronic Quality Management System (eQMS) to ensure compliance with internal procedures and Good Documentation Practices.
- Assist with the initiation, tracking, and documentation of non-conformances.
- Collect data for root cause investigations and support corrective and preventive action (CAPA) tracking and effectiveness checks.
- Update Manufacturing Engineering quality documentation and the ME QA Confluence workspace.
- Compile quality metrics, identify trends, and support continuous improvement initiatives.
- Assist with quality activities for Manufacturing Engineering projects, such as design transfer.
- Collaborate with Manufacturing Engineering, Operations, and Regulatory Affairs teams to communicate project updates.
What you'll need#
- Current enrollment in a recognized Ontario college or university program throughout the co-op term.
- Studies in Quality Assurance, Regulatory Affairs, Biomedical Engineering, Engineering Technology, Life Sciences, Manufacturing Engineering, or a related technical field.
- Proficiency with Microsoft Office applications.
- Strong written and verbal communication skills in English.
- Ability to manage multiple tasks and work both independently and with cross-functional teams.
- Knowledge of ISO 13485 or ISO 9001 is preferred.
- Exposure to eQMS, design transfer, process validation, or CAPA is a plus.
Location & details#
- This position is based in Kitchener, Ontario.
- The role is primarily on-site, with possible remote days depending on business needs and manager approval.
- This is a paid, full-time co-op position.
About Sonova Group
Sonova Group manufactures medical equipment focused on hearing care. The company produces hearing aids, cochlear implants, and wireless communication systems. Its brands include Phonak, Unitron, and Advanced Bionics. Based in Stäfa, the organization operates in over 100 countries and employs more than 10,000 people.
How to get in at Sonova Group
Applying early to Sonova Group gives you a distinct advantage because recruiters review applications as they arrive. Intern Insider sends an instant alert the moment a role matching your target is published, so you can submit your materials before the applicant pile grows. Getting your profile in front of the team early is a standard way to stay competitive. You can also improve your response rates by reaching out to the recruiters behind the roles directly. Intern Insider surfaces the specific people managing these openings, which allows you to ask informed questions or request a referral. Connecting with the right person often helps your application stand out from the crowd.
