Quality Assurance Associate

3 weeks ago


Cambridge, Canada Clarion Medical Technologies 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 with 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 investigate 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.
Post-secondary degree/diploma (Sciences)
- 3-5 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 levels to meet department metrics
- A high level of personal integrity is required
- Excellent communication and interpersonal skills
- Strong problem solving skills and attention to details
- Clarion is an equal-opportunity employer_



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