Bioanalytical QA Associate - Audits & Compliance

Pharma Medica Research Inc.; Canada; On-site; CAD 45,000 - 65,000; Full time

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

Competitive compensation plan

Fully paid benefit plan

Opportunities for advancement

Employee Milestones Awards Program

Corporate Discounts Program

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

Organizational skills

Problem-solving skills

Teamwork

Written and oral communication

Education

B.Sc. degree or Post-Secondary Diploma in scientific, healthcare, or pharmaceutical field

Tools

MS Office

Job description

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.