Tagline:

Contribute towards safe and effective products at a fast-growing medical technology company!

Type of Position:

Full Time

Location:

Kitchener, ON – In office presence required 4-days per week

Benefits:

RRSP with employer match, health benefits (effective day-1!), wellness benefit, learning & development opportunities, paid vacation, personal days, and sick days

The Company Intellijoint Surgical develops effective and easy-to-use products to enhance surgeons’ care and patients’ lives. Today, Intellijoint technology lives in the operating room, helping surgeons improve implant positioning during hip and knee replacement surgeries. Our technology has been used in over 60,000 surgeries. We are seeking a Quality Assurance Analyst to join our Quality Assurance & Regulatory Affairs (QA/RA) team to help bring innovative technologies to the market. The Position Reporting to the Quality and Regulatory Affairs Manager, the Quality Assurance Analyst will support design, production, and process quality. The QA Analyst will contribute to the maintenance of the quality management system ensuring compliance to industry standards and regulatory requirements. This role ensures that our products are safe and effective. Main Duties: Initiate, compose, review, and coordinate cross-functional stakeholders to manage quality issues (e.g. Corrective and Preventative Actions, Deviations, Non-Conformances, etc.) Manage the documentation, investigation, and closure of complaints, including coordination with Regulatory Affairs to determine reportability, as required Provide Operations support (e.g. approval of product records, inspections per material specifications) for the timely release and shipment of product Assist in the maintenance of production processes according to requirements Perform quality assurance activities related to audits, training, change control, document and record management Prepare periodic reports to support the Quality Management System Analyze sources of quality data to identify problem trends and opportunities for improvement Assist in the maintenance, approval, and creation of quality documentation Support planning and execution of design control deliverables Maintain the content of the Design History File to regulatory and customer requirements Participate in the development of new medical device technologies and sustaining engineering projects by providing insight into how quality requirements are met and maintained Skills and Experience to Enable Success: Post-Graduate diploma in Quality Assurance is an asset 3-5 years of relevant quality management experience in a regulated industry Knowledge of Medical Device standards (ISO 13485, MDSAP, ISO 14971, IEC 60601) Working knowledge of root cause analysis tools, CAPAs, Deviations, and NCRs Experience working with software and/or electromechanical products Familiarity with US, Canada, and International Medical Device Regulations Attention to detail and appreciation for process Why Join Us? It is unrealistic for us to believe we will find someone who fits this position 100% Strong support towards career development and growth Work with innovative products that can improve surgical outcomes and enhance patient’s quality of life Be ready to innovate! Work alongside a highly talented and driven group of team members and colleagues organization wide Work in an environment with high transparency and collaboration, along with lots of fun and social activities Be ok with change and share in our excitement as we scale Flexibility so that you can do your best both at work and outside of it Intellijoint Surgical is committed to creating an accessible and inclusive work environment. It is our policy to recruit and select applicants solely on the basis of their qualifications. We are an equal opportunity employer that hires talent regardless of age, race, creed, colour, religion, national origin, ancestry, marital status, sexual orientation, gender identity or expression, disability, or any other status or condition protected by applicable law. Intellijoint Surgical encourages applications from all qualified candidates. Those in need of accommodation at any stage in the recruitment process should notify hr@intellijointsurgical.com. Any information received that relates to accommodation needs of a candidate will be addressed in a confidential manner.

Intellijoint Surgical

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Quality Assurance Analyst