Quality Assurance Associate

Job Description

<p><strong>Introduction</strong></p><p>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. </p><p><br></p><p><strong>Responsibilities</strong></p><p>Quality Assurance Operations:</p><ul><li>Support the execution of quality assurance activities in alignment with GMP (Good Manufacturing Practices), regulatory requirements, and corporate standards.</li><li>Review and approve production records, batch documentation, and certificates of analysis for product release.</li><li>Conduct investigations for deviations, non-conformances, and CAPAs (Corrective and Preventive Actions) to ensure timely resolution and compliance.</li></ul><p>Compliance and Audits:</p><ul><li>Collaborate with cross-functional teams to ensure adherence to regulatory and company quality policies.</li><li>Participate in internal and external audits, including preparation, execution, and follow-up on corrective actions.</li><li>Stay current with industry regulations, guidelines, and best practices to ensure compliance and continual improvement.</li></ul><p>Risk Management and Document Control:</p><ul><li>Perform risk assessments and contribute to quality risk management plans for processes and products.</li><li>Manage and update SOPs (Standard Operating Procedures), work instructions, and other controlled documents in the quality management system.</li></ul><p>Continuous Improvement:</p><ul><li>Support quality improvement projects, including the optimization of QA processes and tools.</li><li>Assist in training programs related to quality systems, regulatory updates, and best practices for internal teams.</li></ul><p><br></p><p><strong>Requirements</strong></p><ul><li>Bachelor's degree in Life Sciences, Biochemistry, Microbiology, Chemistry, or related field.</li><li>2-5 years of experience in a QA or compliance role within the pharmaceutical, biotech, or healthcare industry.</li><li>Strong understanding of GMP, Health Canada regulations, FDA guidelines, and ICH standards.</li><li>Familiarity with quality management systems (e.g., TrackWise, Veeva Vault) is an asset.</li><li>Proficiency in handling documentation, deviation management, and batch record review.</li><li>Excellent organizational skills with the ability to prioritize tasks effectively.</li><li>Strong communication and collaboration abilities to work within cross-functional teams.</li><li>Analytical mindset and attention to detail for problem-solving and ensuring quality compliance.</li></ul><p><br></p><p><strong>What We Offer</strong></p><p>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.</p><p><br></p><p><strong>About Us</strong></p><p>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.</p>