Quality Assurance Associate

3 weeks ago

Toronto, Canada Brunel Full time

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.

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