We are seeking a senior Quality Manager to lead and strengthen quality systems within a regulated pharmaceutical environment. This role will play a key part in maintaining GMP compliance, driving continuous improvement, and supporting manufacturing and supply operations through quality oversight.
Key Responsibilities
* Manage and continuously improve the Quality Management System (QMS) in line with GMP and applicable regulatory requirements
* Lead and oversee deviations, CAPAs, change controls, and risk assessments
* Support internal, supplier, and regulatory audits and inspections, ensuring inspection readiness
* Review and approve quality documentation including SOPs, batch records, validation protocols, and reports
* Partner with Manufacturing, QC, Supply Chain, and Engineering to ensure quality is embedded across operations
* Support training programs and promote a strong quality culture across the site
Required Experience & Qualifications
* Degree in a scientific or technical discipline (or equivalent experience)
* 5+ experience in Quality Assurance within a pharmaceutical manufacturing environment
* Strong working knowledge of GMP and quality systems
* Hands-on experience managing investigations, CAPAs, and change management
* Confident communicator with the ability to influence cross-functional teams
What We're Looking For
* Proactive, detail-oriented quality professional
* Comfortable operating in a fast-paced, regulated environment
* Strong problem-solving skills and ability to balance compliance with operational needs
Why Join
* Opportunity to make a meaningful impact on product quality and patient safety
* Collaborative, quality-driven environment
* Competitive compensation and professional development opportunities