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Strong fit if you want hands-on GMP upstream biologics at a large CDMO in Madison—not remote—and care more about process execution than early R&D science.
As Biomanufacturing Upstream at Catalent Madison, expect cell-culture and bioreactor work supporting biologic production: media prep, inoculum expansion, process monitoring, batch records, and handoff to downstream under GMP.
Prioritize aseptic technique, bioreactor operation, cell culture basics, GMP documentation, and deviation awareness. No cert list was provided for this family.
No. The listing is on-site in Madison, Dane County (remote = 0).
It manufactures and develops medicines and biologics as a global CDMO, with many FDA-supported products historically.
No certification resources or costs were supplied for this occupation family.
Website: catalent.com
Catalent, Inc., is an American pharmaceutical company headquartered in Tampa, Florida.It operates as a privately held independent subsidiary of Novo Holdings A/S. It is a provider of drug delivery technologies, drug development, drug manufacturing, biologics, gene therapy, and consumer health products. It has over 50 facilities on four continents and has supported more than half the products approved by the Food and Drug Administration in the last ten years. Annually, it produces 70 billion doses for 8,000 products. The company's major customers include Bayer, Bristol-Myers…
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Supervisor - Biomanufacturing, Upstream at Catalent in Madison, Dane County Role Overview Catalent is seeking a Supervisor for its biomanufacturing upstream operations based in Madison, Wisconsin. This role will be pivotal in overseeing the upstream processes of mammalian cell line engineering and drug substance biomanufacturing at our state-of-the-art facility. Day-to-Day Responsibilities Supervise and coordinate the day-to-day activities of the upstream biomanufacturing team Ensure compliance with Good Manufacturing Practices (GMP) and all relevant regulatory standards Develop, implement, and maintain efficient operational procedures for cell line engineering and drug substance production Monitor quality control processes to ensure product safety and efficacy Provide technical support and guidance to team members on best practices and troubleshooting Participate in the continuous improvement of biomanufacturing processes Requirements Minimum 5 years of experience in upstream biomanufacturing, preferably within a GMP environment Demonstrated leadership and supervisory skills with a track record of managing teams effectively Strong understanding of mammalian cell culture processes and biopharmaceutical manufacturing Familiarity with regulatory requirements for biologics development and manufacturing Experience in GMP compliance, documentation, and quality assurance practices Bachelor’s degree in Biotechnology, Biology, or a related field; advanced degree preferred More About Catalent Catalent is a global leader in drug development and delivery technologies. Our Madison site specializes in biologics development and manufacturing, supporting customers from research through early- and mid-stage clinical production. Next Steps To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there. Please ensure all required information is accurate and up-to-date for a smooth application process.
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