Job Description

SteriPro Canada

is a leading provider of medical device reprocessing, delivering high-quality sterilization services from our Mississauga facility and on-site at partner hospitals. We adhere to the

Canadian Standards Association (CSA)

requirements and are committed to continuous improvement in the field of Medical Device Reprocessing.

We are seeking an experienced

Production/Site Supervisor

for our partner hospital in Ontario. The successful candidate will complete training at our Mississauga facility before placement. This role oversees daily operations, ensuring safety, quality, and productivity within a unionized environment.

MAIN DUTIES

Supervise and support MDR Technicians in all reprocessing areas. Oversee daily staffing, schedules, and workflow assignments. Ensure all devices are reprocessed according to

CSA

and manufacturer standards. Maintain working knowledge of reprocessing equipment and tracking systems. Conduct daily quality audits and report variances or non-conformances. Monitor instrument repairs, maintenance, and inventory requirements. Enforce health, safety, and PPE compliance. Mentor staff and address attendance, performance, and discipline issues. Participate in special projects, committees, and improvement initiatives.

QUALITY ASSURANCE RESPONSIBILITIES

Ensure adherence to

CSA

, PIDAC, and internal quality standards. Perform QA audits, review sterilization records, and validate documentation. Lead corrective/preventive action (CAPA) processes for identified issues. Collaborate with the Quality team to maintain accurate, compliant records. Support accreditation and regulatory audits.

EDUCATOR RESPONSIBILITIES

Develop and deliver training for new and existing staff. Maintain up-to-date competency checklists and training records. Provide ongoing education on CSA standards, infection control, and safety. Support staff development through mentorship and refresher sessions. Coordinate training for new equipment, technology, or processes.

HEALTH & SAFETY COMPLIANCE

Conduct safety inspections and enforce workplace safety policies. Ensure completion of required training, including

WHMIS

. Promote a proactive safety culture and lead by example.

QUALIFICATIONS

2-5 years of supervisory experience, preferably in medical device reprocessing or healthcare.

MDRAO Certification

required or willingness to obtain.

CMDRS designation

an asset. Strong leadership, organizational, and communication skills. Knowledge of infection control, sterilization processes, and reprocessing equipment. Proficiency in Microsoft Office and scheduling applications. Familiarity with occupational health and safety practices.
Job Type: Full-time

Pay: $60,000.00-$85,000.00 per year

Benefits:

Dental care Disability insurance Extended health care Life insurance Paid time off Vision care
Ability to commute/relocate:

Greater Sudbury, ON: reliably commute or plan to relocate before starting work (required)
Licence/Certification:

MDRAO certification (preferred)
Work Location: In person