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Bioanalytical QA Associate - Audits & Compliance
Job summary
A Contract Research Organization is seeking a QA Associate in Mississauga, Ontario. The role involves preparing and conducting audits for compliance with GLP and GCP regulations, ensuring quality objectives are met and supporting all PMRI divisions. Candidates should have a relevant degree, excellent communication skills, and the ability to work in a team environment. A competitive compensation and benefits package is offered.
Benefits
Qualifications
- 0-3 years of experience in quality assurance, quality control or laboratory role.
- Good understanding of Health Canada, FDA, EU, ICH GLP and GCP regulations.
- Ability to multi-task and keep organized.
Responsibilities
- Prepare and conduct audits of bioanalytical and laboratory activities.
- Audit final study reports for compliance with GCP.
- Report findings to management and ensure corrective actions are implemented.
Skills
Education
Tools
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.