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Head of Manufacturing

Job in Kitchener, Ontario, Canada
Listing for: Qidni Labs
Full Time position
Listed on 2026-09-13
Job specializations:
  • Engineering
    Manufacturing Engineer, Medical Device Industry, Quality Engineering
  • Manufacturing / Production
    Manufacturing Engineer, Medical Device Industry, Quality Engineering
Salary/Wage Range or Industry Benchmark: 120000 - 180000 CAD Yearly CAD 120000.00 180000.00 YEAR
Job Description & How to Apply Below

Qidni Labs Inc. is a medical device company focused on revolutionizing dialysis technology for patients with kidney failure. The technology promises to miniaturize the dialysis machine and reduce the amount of fluid required for treatment, making life-sustaining treatment more accessible globally. Enhancing the patient experience and improving quality of care is the top priority.

Role Overview

This is a full-time, on-site role located in Kitchener, ON. As the Head of Manufacturing, the candidate will lead the development and scaling of Qidni Labs’ manufacturing operations for its blood purification devices.

Responsibilities include establishing manufacturing processes, overseeing production planning and quality systems, coordinating supplier and contract manufacturing relationships, and supporting the transition from prototype to commercial-scale production. The role will require working cross-functionally with engineering, regulatory and quality teams to ensure manufacturing processes meet regulatory and operational requirements.

The ideal candidate will have experience building manufacturing operations within the medical device or regulated healthcare industry and be comfortable working in a fast-paced startup environment.

Qualifications
  • Bachelor’s or Master’s degree in Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, Biomedical Engineering or a related discipline
  • Proven capabilities in manufacturing leadership, preferably within medical devices or regulated industries
  • Experience developing and scaling manufacturing processes from prototype to commercialization
  • Strong knowledge of GMP, ISO 13485, and medical device manufacturing standards
  • Experience managing suppliers, contract manufacturers, and production workflows
  • Excellent organizational, leadership, and problem-solving skills
  • Ability to work cross-functionally with engineering, regulatory, and quality teams
  • Experience with clean room operations is an asset
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