Quality Assurance Associate

1 week ago


Cambridge, Ontario, Canada Clarion Medical Technologies Inc. Full time

The successful applicant will:

  • Experience working in a Good Manufacturing Practice (GMP) environment, as well as a good understanding of GMP principles
  • Facilitate Batch releases and maintain compliance to Health Canada requirements
  • Help maintain day to day and annual GMP/QMS corporate requirements.
  • Ensure customer complaints are received and processed appropriately and consistently to meet regulatory requirements
  • Manage the Corrective Actions / Preventative Actions processes for all products in accordance with established company procedures including receiving, investigating and closing product complaints
  • Manage Quarantined inventory and investigating root origins to meet mínimal threshold allowances
  • Complete key projects within the quality system such as traceability, vendor reviews, temperature monitoring, batch work processing and receiving inspections
  • Facilitate continual improvement of Clarions Quality Systems
  • Postsecondary degree/diploma (Sciences)
  • 35 years experience in Quality role
  • Basic knowledge of statistics desired
  • Post Market Surveillance experience is an asset
  • Ability to work independently
  • Flexible and strong organizational skills to manage time and productivity level to meet department metrics
  • High level of personal integrity is required
  • Excellent communication and interpersonal skills
  • Strong problem solving skills and attention to details


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