Team Lead, GMP Storage

Team Lead, GMP Storage

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.

Catalent's Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services, and Clinical Supply Services businesses. The site provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to clinical and commercial-scale manufacture. The Kansas City facility is a Center-of-Excellence for our Biologics Analytical Services business. Our talented team has over 25 years of experience providing analytical services for stand-alone and integrated biologics projects.

The Team Lead, GMP Storage role is responsible for overseeing daily operations of GMP storage facilities, ensuring full compliance with cGMP requirements while leading a team to safely manage, safeguard, and accurately track all GMP materials from receipt through finished goods completion. The Team Lead, GMP Storage role will be responsible for leading, training, and mentoring storage and warehouse staff to maintain high performance and adherence to SOPs.

This is a full-time, on-site salary position at our Kansas City, Missouri location. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee.

The Role

• Lead, train, and mentor storage and warehouse staff to maintain high performance and adherence to SOPs. Coordinate receipt, inspection, labeling, and storage of GMP materials, including raw materials, intermediates, and finished goods.
• Manage inventory accuracy through regular cycle counts, reconciliations, and timely system updates in ERP system. Ensure proper segregation and handling of quarantined, released, rejected, and returned materials.
• Collaborate with Quality Assurance and Manufacturing teams to resolve deviations, CAPAs, and audit findings. Prepare for and actively participate in internal and external audits / inspections, providing accurate documentation and responses.
• Develop and update SOPs, work instructions, and training materials to reflect current best practices and regulatory requirements.
• Identify and implement process improvements to increase efficiency, reduce errors, and support continuous compliance.
• Coordinate with vendor to dispose of inventory materials appropriately.
• All other duties as assigned.

The Candidate

Why you should join Catalent

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.

Catalent is an Equal Opportunity Employer, including disability and veterans.