QA Associate - Product Release (Hybrid)

Resolute Workforce Solutions; Toronto; Hybrid; CAD 70,000 - 100,000; Full time

Job summary

A leading company specializing in project delivery and quality management is seeking a highly motivated QA Associate - Product Release in Toronto. The role involves reviewing batch records, ensuring regulatory compliance, and releasing pharmaceutical products. This position offers a hybrid work model and opportunities for career growth within a dynamic environment.

Benefits

Health Insurance

Retirement Plan

Paid Time Off

Professional Development Opportunities

Qualifications

• 6–9 years of relevant experience in the pharmaceutical industry.
• Familiarity with GMP guidelines and regulatory compliance.
• Must provide evidence of qualifications per the 2018 GMP Guidelines.

Responsibilities

• Review and assess executed batch records, stability data, and APQRs.
• Release pharmaceutical products and APIs after thorough documentation review.
• Maintain and utilize QA databases and the SAP system.

Skills

Attention to Detail

Analytical Skills

Knowledge of GMP Guidelines

Education

Degree in Chemistry, Biology, or related field

Job description

Resolute Workforce Solutions (Staff augmentation subsidiary of Brevitas Consulting Inc.) is dedicated to helping organizations achieve tangible results and lasting improvements via successful project delivery, continuous process improvement, and effective management of change. Our expertise is in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Project Management.

We are looking for a highly motivated and energetic individual to join our team as a QA Associate - Product Release in Toronto, ON (Hybrid).

Responsibilities :

• Review and assess executed batch records, stability data, and APQRs.
• Release pharmaceutical products and APIs after thorough documentation review.
• Maintain and utilize QA databases and the SAP system.
• Assemble and review batch files for compliance with GMP and regulatory standards.
• Support completion of Annual Product Reviews.
• Perform general administrative tasks related to quality assurance.

Qualifications :

• in Chemistry, Biology, or a related scientific field from a Canadian institution or one recognized by a Canadian accreditation body.
• 6–9 years of relevant experience in the pharmaceutical industry, specifically in QA roles.
• Familiarity with GMP guidelines and regulatory compliance.
• Must provide evidence of qualifications per the 2018 GMP Guidelines.
• Experience with releasing products and APIs to the Canadian market after completing all necessary documentation reviews.

Benefits :

Upon successful completion of probation, you will also be enrolled in our benefit programs :