New · posted Nov 12
Catalent · Pharmaceuticals
Manager, Regulatory Compliance
- Kansas City, MO
- On-site
- Full-time
- Manager
The role
We have an opportunity for a Manager, Regulatory Compliance to join our team. This role manages site regulatory compliance processes, including reporting, licensing support, Quality Technical Agreements, and documentation such as the Site Master File and Quality Manual. The position collaborates with Quality, Operations, Regulatory Affairs, Supply Chain, and Engineering teams to support inspections, fulfill commitments, and drive continuous improvement. The Manager also leads and develops Regulatory Compliance personnel to ensure objectives are achieved in line with regulatory requirements and current Good Manufacturing Practices.
Shift: M-F 8am-5pm
Location: Kansas City, MO
100% Onsite
- Lead and maintain site regulatory compliance programs to ensure adherence to applicable requirements, commitments, company standards, and current Good Manufacturing Practices.
- Manage regulatory submissions, commercial data reporting, licensing activities, and maintenance of regulatory records supporting site operations.
- Own and maintain the Site Master File and Quality Manual, ensuring documents remain current, accurate, and compliant.
- Develop, review, negotiate, approve, and maintain Quality Technical Agreements with customers, suppliers, contract manufacturers, and business partners.
- Support regulatory agency, customer, and pre-approval inspections through documentation preparation, coordination of responses, and follow-up activities.
- Coordinate and track inspection observations, commitments, and corrective action plans to ensure timely completion and sustained compliance.
- Partner with Quality Systems, Manufacturing, Engineering, Supply Chain, and Regulatory Affairs to support investigations, change controls, CAPAs, risk assessments, and compliance improvement initiatives.
- Monitor emerging regulatory requirements, industry trends, and guidance documents to assess potential impacts on site quality systems and operations.
- Lead, coach, develop, and manage Regulatory Compliance personnel, including performance management, employee development, and resource allocation.
- Perform other duties as assigned.
What you need
Minimum Requirements
- Bachelor’s degree in Chemistry, Biology, Pharmaceutical Sciences, Engineering, or a related scientific discipline.
- Minimum five years of experience in pharmaceutical, biotechnology, API manufacturing, quality assurance, regulatory compliance, or another regulated industry.
- Experience with regulatory submissions, site licensing activities, and regulatory reporting.
- Experience working within current Good Manufacturing Practice-regulated environments.
- Experience supporting FDA and/or international regulatory inspections.
- Minimum two years of direct people management experience, including employee coaching, performance management, and development.
- Strong knowledge of pharmaceutical regulations, current Good Manufacturing Practices, quality systems, and regulatory compliance requirements applicable to pharmaceutical and API manufacturing.
- Demonstrated expertise in regulatory submissions, reporting, licensing activities, and management of regulatory documentation, including Site Master Files and Quality Manuals.
- Strong understanding of inspection support activities, regulatory commitments, CAPAs, change controls, investigations, risk management, and continuous improvement processes.
- Excellent leadership, communication, negotiation, and influencing skills, with the ability to partner across functions and manage relationships with customers, suppliers, and regulatory stakeholders.
- 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 & Backgroundnice to have
- Experience managing Site Master Files and Quality Manuals.
- Experience with Quality Technical Agreements.
Pay and benefits
Catalent didn't publish pay for this role
See what similar roles pay on Regulatory Jobs, or try the salary calculator.
Medical, dental, and vision benefits effective day one
Competitive paid time off
8 paid holidays
Tuition reimbursement
Defined career path and annual performance review
Community engagement and green initiatives
Where you'll work
Kansas City, MOOn-siteOpen in Maps (opens in a new tab)
More jobs in Kansas City, MO
From the posting
About Catalent
About Site
Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses.
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.
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 [email protected] 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.
Equal opportunity, accessibility and legal noticesCatalent's statements, word for word
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.
Job intelligence
The context around this role
Live data · November 12, 2026
Salary intelligence
How the pay compares
Manager roles in the US11 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| All US (middle half) | $154,000 | $162,500 | $192,250 |
Comparisons: the base pay employers published on open Compliance roles at the same level on Regulatory Jobs, November 12, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Compliance
The general path across 40 open Compliance roles on Regulatory Jobs, with the titles they carry most. Not Catalent's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 25 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- GMP and compliance11
- Quality systems and risk7
- Documentation and SOPs6
- Collaboration and leadership6
- Regulatory submissions4
- Investigations and CAPA2
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Compliance work in pharmaceuticals, led by the one this posting names, each linked to the agency or standards body that publishes it.
- FDA21 CFR Parts 210 and 211(official source, opens in a new tab)FDA current good manufacturing practice for finished pharmaceuticalsNamed in the posting
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- FDAFDA data integrity guidance(official source, opens in a new tab)Data Integrity and Compliance With Drug CGMP: Questions and Answers
- FDAFDA Investigations Operations Manual(official source, opens in a new tab)How FDA investigators plan and conduct inspections
- ICHICH Q9(R1)(official source, opens in a new tab)Quality risk management
- FDAFDA quality agreements guidance(official source, opens in a new tab)Contract Manufacturing Arrangements for Drugs: Quality Agreements
- HHS-OIGHHS-OIG General Compliance Program Guidance(official source, opens in a new tab)The federal government's guide to healthcare compliance programs and the anti-kickback statute
- FDA21 CFR Part 7(official source, opens in a new tab)FDA enforcement policy, including product recalls
- EUEU GMP (EudraLex Volume 4)(official source, opens in a new tab)The EU's good manufacturing practice rules, including Annex 1 sterile and Annex 15 validation
- ICHICH Q10(official source, opens in a new tab)The pharmaceutical quality system across the product lifecycle
- PIC/SPIC/S(official source, opens in a new tab)The Pharmaceutical Inspection Co-operation Scheme and its GMP guide
- FDADrug Supply Chain Security Act(official source, opens in a new tab)Product tracing, verification and serialization across the US drug supply chain
- ISOISO 19011(official source, opens in a new tab)Guidelines for auditing management systems
- CMSOpen Payments (Sunshine Act)(official source, opens in a new tab)Reporting of manufacturer payments to physicians and teaching hospitals
- DOJForeign Corrupt Practices Act(official source, opens in a new tab)US anti-bribery rules for dealings with foreign officials
- ICHICH E6(R3) good clinical practice(official source, opens in a new tab)The international standard for the design, conduct and reporting of clinical trials
Company hiring pulse
Catalent on Regulatory Jobs
- 38
- Open roles
- 38
- Distinct roles
- 9
- Locations
By discipline
- Quality37 97%
- Regulatory1 3%
By level
- Associate & Specialist16 42%
- Senior & Principal14 37%
- Manager6 16%
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Manager, Regulatory Compliance at Catalent
Applications close December 11.