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About the role
Key responsibilities & impact- Build and standardize scalable manufacturing systems, documentation, and workflows
- Drive the transition of product designs into manufacturable, production-ready systems
- Identify failure modes, resolve root causes, and use production data to improve yield
- Ensure manufacturing processes align with QMS and regulatory requirements
- Collaborate closely with manufacturing partners to align execution with process intent
Requirements
What you’ll need- 5+ years experience manufacturing medical devices
- Strong understanding of DFM, process control, yield improvement, root cause analysis
- Experience developing SOPs, MPIs, structured workflows, and controlled documentation within QMS-regulated environments
- Familiarity with SolidWorks or equivalent CAD tools
- Open to frequent travel to Toronto
Benefits
Comp & perks- Significant equity opportunities
- Startup benefits with a secure product line
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
manufacturing systemsdocumentationworkflowsDFMprocess controlyield improvementroot cause analysisSOPsMPIsQMS
Soft Skills
collaborationproblem-solving
