Associate Director, QMS & Compliance
Catalent · Wiltshire, UK
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Role summary
Catalent seeks an Associate Director to lead quality management systems and regulatory compliance at its Swindon facility. The role involves managing QMS operations, overseeing regulatory affairs, and directing teams to ensure GMP and FDA compliance while driving continuous improvement.
What they're looking for
- Degree in Pharmaceutical Sciences, Chemistry, Physical Sciences, or related field
- Significant pharmaceutical industry experience with demonstrated leadership capability
- Strong customer focus and stakeholder management skills with client-facing experience
- Expertise in problem-solving, risk management, and change management
- Proven ability to lead, develop, and motivate teams effectively
What you'll be doing
- Lead and maintain Quality Management System ensuring GMP, FDA, MHRA compliance
- Oversee regulatory affairs including filings, DMF maintenance, and authority enquiries
- Manage QMS budgets, resources, and drive continuous improvement programs
- Develop and coach high-performing team with succession planning focus
- Partner with customers and stakeholders to support quality and business objectives
Privacy & handoff
This role links to Catalent's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.