Quality Assurance Associate

Quality Assurance Associate III (6-month contract)

Toronto, ON

Introduction

We are hiring a Quality Assurance Associate III for our client based in Toronto, Ontario. The Quality Assurance Associate will be responsible for Quality Compliance and Product Quality related activities for the company’s importation and distribution portfolio. Contribute to establishing and maintaining high quality and compliance status of all products to meet all Canadian cGMP regulations, as well as corporate requirements. This is a 6-month contract position.

Responsibilities

Serve in a backup capacity to other Quality Specialists for their respective responsibilities and coordinate daily, weekly and monthly release activities.

Collect, review and approve all required documentation necessary for product release, including batch documentation review.

Perform periodic (eg. Annual) compliance requirements such as executed batch record review, stability review, APQR etc.

Release products and APIs on Canadian market after completing necessary document review.

Send products for testing, approve results and support laboratories, if required

Complaint Officers in the following capacity as required.

Monitors and tracks sample receipt from complaints.

Performs QC Checks

Understands Health Canada complaint regulations for drug products and medical devices

Supports trending reports

Provides complaint support to other company departments including Customer Service, Medical Information, Pharmacovigilance, Sales Associates, Regulatory, Commercial Operations, Legal, and Risk Management

Participates on ad-hoc teams regarding product-specific complaint issues

Coordinates feedback to customers regarding complaint investigations via QA Coordination Call Center

Participate and support Regulatory Inspections (Health Canada), as well as internal and corporate audits, as required

Participate and support Self-inspection Program

Support Quality Performance Indicators for QA activities

Other QA duties, as assigned

Requirements

B.Sc. in Chemistry, Biology or related sciences from a Canadian University or formal certificate of equivalency*

Minimum of 3 to 5 years of related experience within the pharmaceutical industry.

Experience performing compliance requirements such as executed batch record review, stability review, APQR etc.

Experience with released products and APIs on the Canadian market after completing the necessary document review

What We Offer

Why apply through Brunel? Finding the next step in your career can be a fulltime job in itself. We manage the process for you: from submitting your resume to coordinating interviews to extending offers and assisting with on-boarding. We’ll get you going while you get on with the job.

About Us

Brunel has a reputation for working with some of the best in the business. That’s what we continually strive for. Over 45 years, we’ve created a global network of interesting clients and talented individuals working together through a vast array of services.