Jobs › Catalent

Manager - Quality Assurance, Operations

Catalent · Madison, WI · Full time

Posted Sep 23, 2026 · We last checked this listing on Oct 6, 2026

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Likely interview questions for this role

Written from this job description, not a generic list. Each one notes what the interviewer is really checking.

About your past

This team covers tech transfer, master batch record review, on-the-floor support, product disposition and shipping. How would you organize the team to cover all of that?

What they are checking: Whether they can plan coverage and priorities across many QA Operations functions.

Tell me about a time you coached someone on your team through a hard situation.

What they are checking: Whether they develop people through real coaching, which the posting emphasizes.

Tell me about a time you had to address a team member's performance concern promptly.

What they are checking: Whether they act on performance issues early instead of letting them grow.

What would you do

A client urgently needs a batch shipped, but an open deviation is not closed. What do you do?

What they are checking: Whether they hold release standards while exploring proper paths like risk assessment with the client.

Your floor QA team and manufacturing keep clashing. How do you fix the relationship?

What they are checking: Whether they can build partnership without weakening the QA role on the floor.

About the work

What do you look for when reviewing a master batch record for a newly transferred process?

What they are checking: Whether they check that critical steps, ranges and controls match the process and protect the product.

Walk me through what must be complete before you would approve a product for disposition.

What they are checking: Whether they understand that release depends on batch records, testing, deviations and changes all being closed.

How do you set clear goals for QA staff and know whether they are meeting them?

What they are checking: Whether they manage performance with clear expectations and regular feedback rather than annual surprises.

What metrics would you track for QA Operations, and how would you use them to improve?

What they are checking: Whether they track review cycle time and right-first-time and use them to drive real change.

How do you make sure product is shipped under the right conditions and with the right documents?

What they are checking: Whether they understand cold chain and shipping documentation as part of quality, not an afterthought.

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The full job description

As published by Catalent.

Manager - Quality Assurance (QA), Operations Position Summary: • Work Schedule: Monday – Friday, core hours 8am-5pm • 100% on-site (Madison, WI) 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. The Manager for QA Operations has oversight of the team activities involving manufacturing areas, including process technology transfer, master batch record review and approval, on-the-floor support, product disposition, and shipping. You will be a key member in the growth and development within your department. The Role: • Lead, coach, and develop team members by setting clear goals, monitoring performance, delivering feedback, and addressing performance concerns promptly • Build and support employee capability through targeted training, mentorship, and career‑development planning • Ensure compliant execution of all CGMP and Quality Management System (QMS) requirements across manufacturing and quality control operations, including tracking metrics and driving process improvements • Serve as a primary Quality interface with clients, managing communication, sustaining strong quality relationships, and ensuring alignment with client expectations • Ensure adequate Quality resources are available to support GMP operations, including technology transfers, batch execution, and achievement of site performance targets • Oversee change control processes, audit readiness, and audit responses, including the development and implementation of corrective and preventive actions (CAPAs) • Recruit, develop, and lead a high‑performing Quality team, aligning personnel development and motivation with department and site strategic objectives • Champion continuous improvement initiatives and communicate Quality expectations across the site, including leading cross‑functional efforts and delivering periodic GMP and focused trainings while maintaining a safe, compliant work environment • Other duties as assigned The Candidate: • Bachelor’s degree minimum is required in a STEM discipline plus a minimum of 9 years of relevant GMP experience in QA Operations with at least 4 years in a leadership capacity • We will also accept a Master’s degree with 7+ years OR a PhD with 4+ years of relevant experience • Must be able to ensure data integrity and full compliance with company SOPs, specifications, cGMP, ICH, FDA, and EMA requirements, while integrating and interpreting data across multiple disciplines while commanding the full Biologics process • Demonstrated ability to communicate complex technical information to non‑technical audiences and lead challenging discussions with customers and team members to drive issues to effective resolution • Must be experienced in most aspects of drug development and life cycle support, and able to develop useful strategies and tactics to meet regulatory milestones. • 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 • Physical requirements: Individual must be able to see, hear, read, and write clear English. 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. 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! 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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