Primary Responsibilities:

• The main responsibilities will be to: Audit the manufacturing sites of our clients' suppliers per Pro QC checklists.
• Communicate findings with the audit team and issue audit report within due day.

Certifications Requirements:

• ISO 13485:2016

Industry Experience:

• Medical Devices, cosmetics, natural health products, and pharmaceutical manufacturing Experiences

Job Type: 1099 Contract - Part Time/ One Project at a time
Work Duration/ Shift Hours: 8 hours a day; Current Project 2 days per Audit.
Once one project needs ends, contractor will do other Audits/ Inspections in Ontario area.