FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Manufacturing Engineering QA Co-op
Sonova Group. Support the review, approval routing, formatting and revision control of quality system documents .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates proficiency in Quality Management Systems, including eQMS and Good Documentation Practices, while effectively collaborating with cross-functional teams to support quality assurance initiatives and continuous improvement efforts.
Highest-signal resume keywords
Quality Management System (eQMS)Good Documentation PracticesISO 13485Corrective and Preventive Action (CAPA)Manufacturing Engineering
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Quality AssuranceRegulatory AffairsBiomedical EngineeringEngineering TechnologyLife SciencesManufacturing EngineeringData CollectionRoot Cause InvestigationQuality Metrics CompilationProcess Validation
Soft Skills
OrganizedDetail-OrientedStrong Written CommunicationStrong Verbal CommunicationCollaboration
Tools & Technologies
Microsoft OfficeConfluence
Industry Keywords
Non-ConformanceDesign TransferContinuous ImprovementQuality MetricsCross-Functional Teams
About the role
Key responsibilities & impact- 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
- Support updates to Manufacturing Engineering quality documentation and the ME QA Confluence workspace
- Assist with the initiation, tracking and documentation of non-conformances
- Collect data for root cause investigations and support corrective and preventive action (CAPA) tracking, records and effectiveness checks
- Help compile quality metrics, identify trends and support continuous improvement initiatives
- Assist with quality activities related to Manufacturing Engineering projects, including design transfer
- Collaborate with Manufacturing Engineering, Operations, Quality and Regulatory Affairs teams, and communicate project updates
Requirements
What you’ll need- Currently and actively enrolled in a recognized Ontario college or university program throughout the co-op placement; applicants who have already graduated are not eligible
- Studying Quality Assurance, Regulatory Affairs, Biomedical Engineering, Engineering Technology, Life Sciences, Manufacturing Engineering or a related technical discipline
- Organized, detail-oriented and able to manage multiple tasks reliably
- Strong written and verbal communication skills in English
- Comfortable working independently and collaborating with cross-functional teams
- Proficient with Microsoft Office applications
- Knowledge of ISO 13485 or ISO 9001 is an asset
- Exposure to eQMS, design transfer, process validation, non-conformances or CAPA is an asset
Benefits
Comp & perks- Possible remote days depending on business needs, assigned responsibilities and manager approval
- Equal employment opportunity
- Diverse and inclusive workplace