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A global leader in infection control solutions is seeking a Quality Engineer for their new manufacturing plant in London, Ontario. This role involves implementing the Quality Management System (QMS), collaborating with teams to ensure compliance, and conducting audits. The ideal candidate has 3+ years of quality experience, a degree in a relevant field, and strong communication skills. Attractive compensation and benefits are offered.
About the Company
At Caméléon RH, we believe recruitment is all about alignment; between a person, a company, and a work environment. That’s why we take the time to deeply understand the people behind the CVs and the workplaces behind the job titles.
Our client, Manikheir, is a global leader in infection control solutions. For over 30 years, Medicom has manufactured and distributed high-quality, single-use products for the medical, dental, industrial, veterinary, and retail sectors. With operations across North America, Europe, and Asia, Medicom is now launching a new nitrile glove production facility in London, Ontario, and they’re looking for passionate people to join the mission.
You'll be part of a collaborative and dynamic team committed to health, safety, and quality. This new facility offers a unique opportunity to contribute to the early stages of a growing operation. Medicom promotes autonomy, accountability, and continuous improvement in a structured and regulated manufacturing environment.
As a Quality Engineer, you will:
Support the implementation and maintenance of the Quality Management System (QMS) in compliance with ISO 13485 and regulatory requirements
Collaborate with cross-functional teams (Engineering, Production, Manufacturing) to ensure product quality and compliance
Manage QMS documentation: Medical Device Files, Change Requests, Risk Management Files, and Design History Files
Conduct internal audits and prepare for external audits
Lead investigations into Non-Conformances (NCRs) and drive effective corrective actions (CAPA)
Provide training on quality procedures and tools (eQMS, MES)
Participate in validation activities (IQ, OQ, PQ)
Contribute to continuous improvement initiatives
Perform other related duties assigned by the Quality Operations Manager
Minimum 3 years of experience in Quality or a related field
University or college degree in a science, technical, or regulatory discipline
Strong knowledge of CAPA processes and root cause analysis
Experience with NCRs and eQMS systems
Excellent communication skills and ability to train staff
Experience in validation (IQ, OQ, PQ)
Experience in the Medical Device industry
Understanding of ISO 13485 and Canadian medical device regulations
Experience with MES (Manufacturing Execution System)
Experience conducting internal audits
Six Sigma training or ASQ CQE certification
Competitive compensation and full benefits
The chance to grow with a brand-new manufacturing plant
A meaningful mission: helping protect health globally
A supportive, inclusive, and agile team environment