Supervisor, Quality Assurance

Supervisor, Quality Assurance

Position Summary:

Work Schedule:

2nd shift Monday-Friday afternoons

100% on-site

Catalent Madison is a pharmaceutical manufacturing site specializing in the development and production of high-quality drug products, with a strong focus on biologics and sterile injectables. The site supports global clients by delivering compliant, reliable, and scalable manufacturing solutions.

The Quality Assurance Supervisor at Catalent Madison is responsible for ensuring full compliance with FDA regulations and internal quality systems to support the delivery of high-quality drug products. This position leads team performance, oversees daily QA operations, and drives continuous improvement across quality systems, including deviations, CAPAs, document control, materials management, and training. The Quality Assurance Supervisor partners closely with cross-functional stakeholders to maintain efficient processes, support manufacturing operations, and ensure audit and inspection readiness.

Additionally, it is accountable for developing talent, managing performance, and reinforcing a compliant and high-performing quality culture.

The Role:

• Lead, coach, and develop team members to strengthen performance and support career growth
• Set clear goals, monitor progress, and address performance issues with timely feedback
• Oversee daily QA operations to ensure quality standards and project timelines are met
• Partner with stakeholders to maintain efficient processes and ensure compliant quality practices
• Support and execute Quality Management Systems within CGMP manufacturing and QC environments
• Track KPIs, report performance, and implement action plans to close gaps and meet objectives
• Author, review, and approve procedures, protocols, deviations, and investigation records
• Drive continuous improvement initiatives across systems, processes, training, and regulatory readiness
• Manage document control processes, ensuring integrity, compliance, and system enhancements
• Oversee materials quality and training programs, including compliance, onboarding, system management, and cross-functional support
• Other duties as assigned

The Candidate:

• Doctorate Degree in STEM discipline with minimum of 2 years related experience
• Master's, Bachelor's or Associate's Degree in STEM discipline with minimum of 4 years related experience
• Leadership experience 0-2 years
• Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience

Why you should join Catalent:

• Potential for career growth on an expanding team
• Abundance of cross-functional exposure to other areas within the organization
• Opportunity to work globally
• 152 hours of paid time off annually + 8 paid holidays
• Day one benefits! Medical, dental, vision and 401K benefits effective on your first day

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.

Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

Personal initiative. Dynamic pace. Meaningful work.

Catalent is an Equal Opportunity Employer, including disability and veterans.