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Quality Assurance Associate

1 month ago

Greater Toronto Area, Canada Brunel Full time

Introduction

We are currently hiring aQuality Assurance Associate to for our client, a global pharmaceutical company known for its contribution in areas including pharmaceuticals and consumer healthcare products globally. This is a full-time contract with possibility of extension or become permanent.


Responsibilities

Quality Assurance Operations:

  • Support the execution of quality assurance activities in alignment with GMP (Good Manufacturing Practices), regulatory requirements, and corporate standards.
  • Review and approve production records, batch documentation, and certificates of analysis for product release.
  • Conduct investigations for deviations, non-conformances, and CAPAs (Corrective and Preventive Actions) to ensure timely resolution and compliance.

Compliance and Audits:

  • Collaborate with cross-functional teams to ensure adherence to regulatory and company quality policies.
  • Participate in internal and external audits, including preparation, execution, and follow-up on corrective actions.
  • Stay current with industry regulations, guidelines, and best practices to ensure compliance and continual improvement.

Risk Management and Document Control:

  • Perform risk assessments and contribute to quality risk management plans for processes and products.
  • Manage and update SOPs (Standard Operating Procedures), work instructions, and other controlled documents in the quality management system.

Continuous Improvement:

  • Support quality improvement projects, including the optimization of QA processes and tools.
  • Assist in training programs related to quality systems, regulatory updates, and best practices for internal teams.


Requirements

  • Bachelor’s degree in Life Sciences, Biochemistry, Microbiology, Chemistry, or related field.
  • 2-5 years of experience in a QA or compliance role within the pharmaceutical, biotech, or healthcare industry.
  • Strong understanding of GMP, Health Canada regulations, FDA guidelines, and ICH standards.
  • Familiarity with quality management systems (e.g., TrackWise, Veeva Vault) is an asset.
  • Proficiency in handling documentation, deviation management, and batch record review.
  • Excellent organizational skills with the ability to prioritize tasks effectively.
  • Strong communication and collaboration abilities to work within cross-functional teams.
  • Analytical mindset and attention to detail for problem-solving and ensuring quality compliance.


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.