Supervisor - Biomanufacturing, Central Services

About this role

Supervisor - Biomanufacturing, Central Services Role

About Site Catalent’s Madison, Wisconsin site is a state‑of‑the‑art biologics development and manufacturing facility supporting customers from research through early‑ and mid‑stage clinical production. Located at 726 Heartland Trail in Madison, the approximately 102,700‑square‑foot GMP facility specializes in mammalian cell line engineering, drug substance biomanufacturing, and biopharmaceutical development, utilizing flexible single‑use systems to enable rapid scale‑up and customization. The site is home to Catalent’s proprietary GPEx® and GPEx® Lightning technologies, which are used to generate high‑yielding mammalian cell lines for biologic therapies, and supports production scales ranging from 50 to 4,000 liters for clinical manufacturing. Following a $45 million expansion announced in 2025, the Madison site has significantly increased capacity, added new equipment, and created approximately 200 highly skilled biohealth jobs, further strengthening its role within Catalent’s global biologics network and Wisconsin’s growing life sciences ecosystem.

Position Summary We have an opportunity for a Supervisor - Biomanufacturing, Central Services to join our team. In this role, you will oversee biomanufacturing operations in cleanroom environments, ensuring compliance with cGMP standards and production timelines. You will manage equipment operations, documentation, and quality processes while leading audits and supporting regulatory readiness. This position also involves supervising staff, maintaining facilities, and driving continuous improvement initiatives.

Shift: 2nd Shift: 2:00 PM - 12:00 AM Schedule: Sunday–Wednesday Location: Madison, WI 100% Onsite

The Role • Oversee biomanufacturing operations in cleanroom environments, ensuring compliance with current Good Manufacturing Practice (cGMP) standards and production timelines.

• Manage operation and maintenance of manufacturing equipment, including monitoring core systems and ensuring proper functionality.

• Author, review, and approve documentation such as Standard Operating Procedures (SOPs), Batch Production Records (BPRs), and related materials.

• Ensure quality and compliance through documentation review, deviation investigations, and adherence to the Quality Management System.

• Lead audits, serve as a liaison for clients and internal stakeholders, and support regulatory readiness.

• Supervise staff, including training, mentoring, performance management, and leading team meetings or training sessions.

• Oversee facility and operational upkeep, including cleanroom housekeeping, equipment maintenance, and qualification/validation activities.

• Drive continuous improvement initiatives, training program effectiveness, and support change control and process enhancements.

• Other duties as assigned.

The Candidate Minimum Requirements • Bachelor’s or Associate’s degree in a scientific, engineering, or biomanufacturing field with a minimum of 2 years of relevant experience OR

• High School Diploma with a minimum of 5 years of relevant experience

• Physical Requirements: This position requires frequent sitting, standing, walking, reading of written documents and use of computer monitor screen, reaching with hands and arms, talking, writing, listening. Occasional stooping, kneeling, crouching, bending, carrying, grasping. Frequent lifting and/or moving up to 10 pounds and occasional lifting and/or moving up to 50 pounds. Must comply with Environmental Health and Safety (EHS) responsibilities for the position. Working conditions will be Heating Ventilation and Air Conditioned controlled. Ability to operate within a clean room environment as needed.

• 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.

Preferred Skills & Background • GMP experience preferred

Why You Should Join Catalent • Defined career path and annual performance review and feedback process

• Diverse, inclusive culture

• Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives

• Competitive paid time off plus 8 paid holidays

• Community engagement and green initiatives

• Medical, dental and vision benefits effective day one of employment

• Tuition Reimbursement

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. Visit Catalent Careers to explore career opportunities.

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

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.      Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agenc

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