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