Job Description

SciCan is a market leader in the manufacture and distribution of dental and medical equipment. SciCan's manufactured sterilization and disinfection equipment is sold in over 80 countries, worldwide. SciCan is located in Toronto near the intersection of Highways 401 and 404 (Don Mills and York Mills). It is accessible by public transportation.

We currently have an opening for a Quality Control Engineer as part of our Quality Assurance Department. This position i is responsible for the following activities including but not limited to; quality inspection, managing supplier files, analyzing rejected parts and defects, overseeing non-conformance handling, and facilitating communication with suppliers. This position involves diverse quality assurance activities, including process improvement and regulatory compliance activities.

Key Responsibilities:

• Perform in-process inspections and final quality checks according to the schedule.
• Investigate nonconforming parts and recommend resolutions for incoming and in-process rejected components as needed.
• Document rejected materials using the MRR process, collaborating with suppliers to determine dispositions and ensure timely closure of MRR cases.
• Coordinate with the other department on the disposition of rejected parts when necessary.
• Generate quality reports, analyze failures, and propose corrective actions.
• Maintain ongoing communication with suppliers regarding nonconformities.
• Assess and periodically re-evaluate supplier performance according to SOP.
• Ensure regular maintenance of nonconforming parts inventory within the ERP system.
• Conduct scheduled supplier audits.
• Issue supplier corrective action requests based on trend analysis and oversee the proper closure of SCAR activities.
• Provide backup support to other Quality Assurance team members as required.
• Perform additional duties assigned by the QA Manager or Team Lead to support the QA department.

Qualifications & Requirements:

• Degree in Quality Engineering or Engineering Degree plus Quality Certificate
• Minimum of 1-year related experience in a Medical Device manufacturing environment preferably with technology related products
• Interpret and analyze blueprints and engineering drawings.
• Extensive familiarity with ISO 13485, preferably the 2016 version; MDSAP, MDR experience is an asset
• Internal auditing and risk management experience an asset
• Strong communication skills both verbal and written
• Ability to work in groups as well as independently with minimal supervision
• Strong analytical and problem-solving skills are essential
• Ability to lift 20 kg, occasionally
• Computer skills: MS Office, Visio, PLM & ERP (SAP preferred)

Additional Information

We offer :Competitive compensation, comprehensive Benefit & Pension program, continuing education reimbursement program, Fun & Positive team environment, a subsidized cafeteria, wellness programs, and free parking to name a few. You may learn more about SciCan business and products by visiting our website at

We thank all candidates for their interest in SciCan. Candidates that meet the above requirements will be contacted for an interview. No phone calls please.

By applying and submitting your resume to our job posting, candidate acknowledges and confirms that the submitted resume is true and that the candidate is able to provide evidence of academic achievement or other information as required.

SciCan strongly believes that diversity in the workplace is essential to our success. We are committed to providing equal opportunities regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, disability, gender identity and we are committed to accommodating applicants with disabilities throughout the hiring process, in accordance with the Accessibility for Ontarians with Disabilities Act (AODA). Accommodations are available upon request for candidates taking part in all aspects of the recruitment and selection process.

Job Tags

Similar Jobs