Manufacturing Engineering QA Co-op

Sonova
Kitchener
Workplace: HybridInternshipFunction: Manufacturing & Production OperationsSkills: ["Organized","Detail-oriented","Communication","Independent work","Cross-functional collaboration"]

Join the Quality and Regulatory Affairs team to support quality assurance activities in a medical-device manufacturing environment. Help manage quality documentation workflows, maintain records in the electronic Quality Management System (eQMS), and support non-conformance, CAPA tracking, and root-cause data collection. Contribute to quality metrics, trend analysis, and continuous improvement, while collaborating with Manufacturing Engineering, Operations, and QA/RAs on projects including design transfer.

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FursaFursa
Sonova
Sonova
12 hours ago

Manufacturing Engineering QA Co-op

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Source: Company careers pageValidated by: Fursa AI
Last checked: 12 hours agoStatus: Live

Job Summary

Join the Quality and Regulatory Affairs team to support quality assurance activities in a medical-device manufacturing environment. Help manage quality documentation workflows, maintain records in the electronic Quality Management System (eQMS), and support non-conformance, CAPA tracking, and root-cause data collection. Contribute to quality metrics, trend analysis, and continuous improvement, while collaborating with Manufacturing Engineering, Operations, and QA/RAs on projects including design transfer.
Location: Kitchener
Workplace: Hybrid
Employment Type: Internship
Job Function: Manufacturing & Production Operations
Seniority: Intern level

Key Responsibilities

  • •Support the review, approval routing, formatting, and revision control of quality system documents.
  • •Maintain records in the electronic Quality Management System (eQMS) and help ensure documentation follows internal procedures and Good Documentation Practices.
  • •Assist with initiation, tracking, and documentation of non-conformances.
  • •Collect data for root cause investigations and support CAPA tracking, records, and effectiveness checks.
  • •Compile quality metrics, identify trends, and support continuous improvement initiatives, collaborating across teams including Manufacturing Engineering and Quality/Regulatory Affairs.

Key Requirements

  • •Currently and actively enrolled in a recognized Ontario college or university program throughout the co-op placement (graduated applicants are not eligible).
  • •Studying Quality Assurance, Regulatory Affairs, Biomedical Engineering, Engineering Technology, Life Sciences, Manufacturing Engineering, or a related technical discipline.
  • •Organized and detail-oriented with the ability to manage multiple tasks reliably.
  • •Strong written and verbal communication skills in English.
  • •Proficient with Microsoft Office applications.
Skills:OrganizedDetail-orientedCommunicationIndependent workCross-functional collaboration
Languages:English
Tech Stack:Microsoft OfficeEQMSConfluenceISO 13485ISO 9001

Company Brief

Sonova
Designs, manufactures, and distributes hearing care solutions including hearing aids, cochlear implant accessories, and wireless communication devices, serving audiologists and consumers worldwide through clinics, retail networks, and distribution partners.
Industry: Medical Devices
Company Size: Enterprise (1,001+ employees)
Revenue: USD 1B+
Growth: Public Company
Valuation: Public Company (Market Cap in USD)
Funding: IPO / Publicly Listed
Headquarters: Stäfa, Switzerland
Founded: 1947
Website