Regional Supervisor, GO, US

Catalent Pharma Solutions; Kansas City (MO); On-site; USD 85,000 - 110,000; Full time

Job summary

Catalent Pharma Solutions seeks a Regional Supervisor, GO, US for our Kansas City, MO site (or other locations). The role focuses on regional leadership across pre-production, pre-distribution, and master data, ensuring on-time delivery and cross-functional collaboration across sites and time zones.

The successful candidate will lead daily priority discussions, drive continuous improvement, and coordinate with global supervisors to align regional goals with corporate objectives.

Qualifications

• Bachelor’s degree or equivalent professional experience required; APICS certification preferred.
• 3–5 years of experience in clinical trial materials, supply chain, master data, pre-production, pre-distribution, project management, or related operational functions.
• Demonstrated leadership experience; internal Catalent leadership programs may count toward external experience.

Responsibilities

• Serve as regional supervisor for assigned area and collaborate with two other regional supervisors globally.
• Oversee three departments: pre-production, pre-distribution, and master data.
• Lead daily priority discussions with teams and sites within the business unit.
• Participate in continuous improvement projects to support departmental growth.
• All other duties as assigned.

Skills

Leadership

Project management

Supply chain

Education

Bachelor's degree in Biology, Chemistry, Pharmacy, Business, Supply Chain Management, or equivalent

Job description

Regional Supervisor, GO, US

Position Summary:

• Work Schedule: M-F 8am-5pm
• 100% on-site
• This position can sit at our Philadelphia, Kansas City, or San Diego site

Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses.

We have an opportunity for a Regional Supervisor, GO, US to join our team. This role involves working in a dynamic environment with a focus on operational excellence and compliance. You will manage regional priorities, lead teams, and ensure timely execution of deliverables. The position requires strong leadership, organizational skills, and the ability to work across functions and time zones.

The Role:

• Serve as regional supervisor for assigned area and collaborate with two other regional supervisors globally.
• Oversee three departments: pre-production, pre-distribution, and master data.
• Lead daily priority discussions with teams and sites within the business unit.
• Participate in continuous improvement projects to support departmental growth.
• All other duties as assigned.
  

The Candidate:

• Bachelor’s degree in Biology, Chemistry, Pharmacy, Business, Supply Chain Management, or equivalent professional experience. APICS certification preferred.
• Minimum 3-5 years of experience in clinical trial materials, supply chain, master data, pre-production, pre-distribution, project management, or related operational functions, including prior supervisory or team leadership experience.
• 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.

Why you should join Catalent:

• Defined career path with annual performance reviews and feedback process.
• Diverse and 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 [e-mail]. 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 [e-mail] for us to investigate with local authorities.

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