catalent

Supervisor - Biomanufacturing, Central Services

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At a Glance

Location
Madison, Wisconsin, United States
Employment
Full time
Experience
2+ years
Posted
2026-07-16

Requirements

Why you should join Catalent:

Compensation & Benefits

Tuition Reimbursement - Let us help you finish your degree or start a new degree!

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.

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Catalent Careers

Responsibilities

Located in Madison, WI, this facility features advanced mammalian cell line engineering and biomanufacturing capabilities using single-use systems to support scalable production.

Good Manufacturing Practice (GMP) facility offers integrated formulation and analytical services to address complex development challenges in Biologics.

The Manufacturing Execution – Central Services Supervisor leads a team responsible for staging, powder weighing, and solution preparation supporting upstream, downstream, and mRNA biomanufacturing operations.

The role performs and oversees cGMP manufacturing activities, ensuring adherence to SOPs while maintaining compliance in a regulated environment.

Responsibilities also include reviewing batch records and data, preparing technical documentation, supporting investigations and continuous improvement, and supervising 5–15 direct reports including performance management and staffing recommendations.

Oversee biomanufacturing operations in cleanroom environments, ensuring compliance with cGMP standards and production timelines.