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.