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Qidni Labs

Head of Manufacturing

Kitchener, ON, Canada

Full-time

Within 25 km of Cambridge · About 14.2 km from the city centre

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Job details

Job type: Full-time
Apply by: Feb 23, 2027
Posted: Aug 27, 2026

Original job description

Company Overview

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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More about this job

Responsibilities

Lead the development and scaling of manufacturing operations for blood purification devices, transitioning from prototype to commercial-scale production. Establish manufacturing processes and oversee production planning, quality systems, and supplier relationships.

Requirements

Requires a Bachelor's or Master's degree in Engineering and proven leadership experience in medical device or regulated healthcare manufacturing. Must have strong knowledge of GMP and ISO 13485 standards.

Skills

Manufacturing Leadership
Production Planning
Quality Systems
Supplier Management
Contract Manufacturing
GMP
ISO 13485
Clean Room Operations
Cross-functional Leadership
Commercialization
Medical Device Manufacturing
Problem-solving

Visa sponsorship

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Keywords

Medical Devices
Blood Purification
GMP
ISO 13485
Clean Room
Manufacturing Engineering
Mechanical Engineering
Industrial Engineering
Biomedical Engineering
Production Workflow
Commercialization
Regulated Industry
Healthcare Technology
Quality Systems
Supply Chain Management

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