Supervisor - Biomanufacturing, Central Services

Catalent Pharma Solutions; Alabama; On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

PTO + Holidays

401K match

Medical benefits

Tuition reimbursement

Job summary

Catalent, Inc. seeks a Biomanufacturing Supervisor for Central Services in an on-site Madison, WI facility.

You will supervise staging, preparation, and GMP-compliant production activities supporting multiple biomanufacturing streams, including mRNA work, while ensuring document control and continuous improvement. You will review batch records, author technical documents, and lead investigations, coaching 5–15 direct reports and coordinating with QA and operations to meet production timelines

Qualifications

• Bachelor's or Associate's degree in a scientific/engineering/biomanufacturing field, or the equivalent experience.
• Experience with cGMP and regulated environments is preferred.

Responsibilities

• Lead a team of 5–15 in staging, powder weighing, and solution preparation for upstream, downstream, and mRNA biomanufacturing.
• Perform and oversee cGMP manufacturing activities and ensure SOP compliance.

Skills

Team leadership

cGMP knowledge

Documentation accuracy

Problem solving

Education

Bachelor's or Associate's degree in science/engineering/biomanufacturing

Tools

BPR systems

Job description

Position Summary

Biomanufacturing Supervisor, Central Services

Work Schedule

10pm-8am Sunday-Wednesday 100% on-site

Location

Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). Located in Madison, WI, this facility features advanced mammalian cell line engineering and biomanufacturing capabilities using single-use systems to support scalable production. This 263,000 sq. ft. Good Manufacturing Practice (GMP) facility offers integrated formulation and analytical services to address complex development challenges in Biologics.

Responsibilities

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.

Role Overview

Oversee biomanufacturing operations in cleanroom environments, ensuring compliance with 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 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.

Qualifications

The Candidate: 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. GMP experience preferred.

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 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.

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
• 152 hours of PTO + 8 paid holidays
• Generous 401K match
• Medical, dental and vision benefits
• Tuition Reimbursement - Let us help you finish your degree or start a new degree!

EEO Statement

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

Accommodation Notice

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 [e-mail]. This option is reserved for individuals who require accommodation due to a disability.

About Catalent

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.