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Catalent Pharma Solutions LLC

Supervisor - Engineering, Validation

Madison, WI, United States

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Job details

Apply by: Nov 30, 2026
Experience: 0–2 years of leadership experience required.
Posting language: English
Posted: Nov 6, 2026

Original job description

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 - Engineering, Validation to join our team in Madison, WI. This role supports the Quality Assurance department, ensuring compliance with FDA and other regulatory requirements. The position oversees validation programs, including commissioning, qualification, and computer system validation, while maintaining systems in a validated state. The Supervisor will lead a team of validation professionals, ensuring quality, compliance, and continuous improvement across all validation activities.

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

The Role

Lead a team of Validation professionals.
Maintain Validation Master Plans.
Review and approve validation protocols and reports.
Support commissioning, qualification, and validation activities.
Review Change Controls.
Manage requalification programs.
Participate in audits and inspections.
Drive continuous improvement initiatives.
Serve as Validation Subject Matter Expert (SME).
Coordinate with Quality Assurance, Manufacturing, Facilities, Engineering, and customers.
Provide technical training and support.

The Candidate Minimum Requirements

Doctorate degree in a STEM field with at least 2 years of related experience, or Master’s degree in a STEM field with at least 4 years of related experience, or Bachelor’s degree in a STEM field with at least 5 years of related experience.
0–2 years of leadership experience required.
Experience in Commissioning, Qualification, and Validation (CQV).
Knowledge of validation lifecycle management.
Experience with Change Control impact assessments.
Experience in requalification and periodic reviews.
Proficiency in validation protocol and report writing and execution.
Strong understanding of current Good Manufacturing Practices (cGMP).
Knowledge of FDA, ICH, and EMA regulations.
Ability to interpret regulatory guidance and validation requirements.
Experience leading validation projects and initiatives.
Frequent sitting, standing, walking, computer work, and document review.
Occasional bending, kneeling, crouching, and carrying materials.
Frequent lifting up to 10 lbs and occasional lifting up to 50 lbs.
Ability to work within cleanroom environments as needed.

Preferred Skills & Background

Experience in pharmaceutical manufacturing.
Experience in biologics manufacturing.
Experience in biotech manufacturing.
Experience in cell therapy or gene therapy environments.
Experience in Contract Development and Manufacturing Organizations (CDMOs) such as Catalent, Thermo Fisher Scientific, AbbVie, Fujifilm Diosynth, Lonza, CSL Behring, Pfizer, Amgen, Lilly, or Genentech.
Experience supporting biologics operations involving manufacturing processes and validated systems.

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 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.

Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond - it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.

Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.

Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.

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More about this job

Skills

Quality assurance
Regulatory compliance
Lead a team
Process improvement
Inspection
Provide technical training
Leadership
Report writing
Good manufacturing practices
Heavy lifting
Pharmaceutical processes
Manufacturing processes
Community engagement

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