Facilities Manager

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 Manager - Facilities to join our team at Catalent Pharma Solutions in Madison, Wisconsin. This role leads maintenance activities within the Facilities group and supervises a team of maintenance technicians. The position focuses on ensuring maintenance work is completed properly, troubleshooting equipment and facility issues, and supporting investigations related to equipment failures. The successful candidate will help maintain a safe, compliant, and efficient facility environment while developing and supporting their team.

Shift: M-F 8am-5pm
Location: Madison, WI
100% Onsite

The Role

• Lead and support a team of 4–8 maintenance technicians, assigning daily work and priorities.
• Coordinate technician schedules, paid time off, and coverage.
• Train, coach, and conduct performance discussions and development activities.
• Schedule preventive maintenance and prioritize corrective maintenance work orders.
• Coordinate contractor activities and ensure maintenance tasks are completed on time and documented properly.
• Support technicians with complex equipment issues, including HVAC, electrical systems, and facility utilities.
• Serve as the escalation point for unresolved technical problems.
• Review maintenance records and ensure cGMP-compliant documentation.
• Support deviations, investigations, and change controls.
• Write and update standard operating procedures and maintenance procedures.
• Manage outside vendors and contractors, ensuring work quality and safety compliance.
• Recommend facility improvements and repairs to enhance safety, compliance, and efficiency.

The Candidate

Minimum Requirements

• Journeyman-level training or certification in Electrical, Electronics, HVAC, or a related technical trade with at least 5 years of experience, or
• Associate Degree in Electrical, Electronics, or a related field with at least 5 years of experience, or
• Related Military Technical Training with at least 5 years of electrical/electronics experience.
• 3–5 years of leadership or supervisory experience.
• Experience leading maintenance technicians or skilled trades personnel.
• Strong background in facility maintenance, HVAC troubleshooting and repair, and electrical troubleshooting.
• Familiarity with cGMP manufacturing environments.
• Mechanical and electrical aptitude.
• Experience writing and following procedures and standard operating procedures.
• Strong written and verbal communication skills.
• Detail-oriented with strong documentation skills.
• Ability to read, write, and speak English clearly.
• Ability to stand for up to 8 hours per day.
• Ability to work indoors and outdoors as business needs require.
• Frequent sitting, standing, walking, climbing stairs and ladders, reading, writing, speaking, listening, and computer use.
• Occasional bending, kneeling, crouching, reaching, and carrying materials.
• Ability to lift up to 50 pounds regularly and occasionally up to 80 pounds.
• 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

• Pharmaceutical, biotech, or regulated manufacturing experience.
• Knowledge of FDA and GMP regulations (21 CFR 210/211).
• PLC and ladder logic knowledge.
• Experience with cGMP facility construction or startup.
• Experience with audits, deviations, and change controls.

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 [email protected]. 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 agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

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