Job Title

Our client, a company specializing in the distribution and servicing of medical devices, is currently seeking a Quality Assurance and Regulatory Affairs Specialist to join their team.Full time. Permanent.Responsibilities: Manage document control processes: preparation, review, distribution, training, filing, and archiving;Support internal/external audits and related follow-ups;Assist in investigations and root cause analyses of non-conformities;Contribute to corrective/preventive actions and continuous improvement efforts;Help maintain regulatory documentation and support application renewals;Collaborate with teams on quality/regulatory matters and process improvements;Assist with post-market surveillance, including tracking recalls, customer feedback, and complaints;Support supplier qualification and licensing renewals;Contribute to health and safety initiatives;Perform other QA/RA duties as assigned.Profile:Strong communication and teamwork skills;Ability to handle regulatory/quality concerns with professionalism;1+ year in QA/RA;Bachelors in Health Sciences, Engineering, Pharmaceutical or any other related field;Familiarity with ISO 9001, ISO 13485, MDSAP, FDA CFR 820, or SOR 98-282 is an asset;Strong organizational skills; capable of managing multiple priorities;Proficient in Microsoft Office.Benefits:Comprehensive benefits package after 3 months;Access to a wide range of employee programs and resources;3 weeks vacation to start.