Operations Zone Manager - Second Shift

About Site Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. Position Summary We have an opportunity for an Operations Zone Manager - Second Shift to join our team. This role ensures that products are produced with the right quality, cost, and timing while maintaining compliance with cGMP standards. The position focuses on developing strong interdepartmental relationships and driving performance improvements. The successful candidate will lead a team of technicians and collaborate across departments to ensure smooth operations and continuous improvement. Shift: M-Th 1:30pm-12am Location: Kansas City, MO 100% Onsite The Role Manage Pharmaceutical Manufacturing Technicians within the assigned zone, including selection, performance evaluation, counseling, and conflict resolution. Collaborate with Supply Chain, Maintenance, and Quality Assurance to ensure efficient schedules and high-quality products. Oversee daily performance against standards and schedules, resolving workflow and technical issues as needed. Make personnel decisions regarding staffing, wages, and performance reviews while maintaining compliance with cGMP and safety regulations. Ensure the facility remains “tour ready” and that people, materials, and cleaning processes are maintained effectively. Execute training for Technicians on manufacturing and cleaning standard operating procedures and applicable regulations. Oversee personnel allocation to ensure timely project completion and accurate batch records. Provide updates to management and stakeholders on project timelines. Troubleshoot processing, equipment, or utilities issues and support workforce motivation and training. Define and implement Corrective/Preventive Actions in response to audits and deviations, driving process improvements through change control. Support 24/7 operations as needed and perform other assigned duties. The Candidate Minimum Requirements High School Diploma or General Educational Development (GED) required. Ability to create and work within an operating plan framework and budget. Thorough knowledge of equipment and processes used in pharmaceutical manufacturing. Strong understanding of cGMP, Food and Drug Administration (FDA), Medicines and Healthcare products Regulatory Agency (MHRA), European Union (EU), and Drug Enforcement Administration (DEA) guidelines and their application. Knowledge of Solid Dosage manufacturing. Ability to manage priorities and projects effectively, with strong communication and people management skills. Excellent computer skills. Ability to work effectively in a matrix organization. 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 & Background Five years of prior supervisory or relevant management experience (e.g., pharmacy, chemistry, or science) preferred. Why You Should Join Catalent Defined career path with annual performance reviews and feedback. Diverse and inclusive culture. Opportunities for career growth within an organization dedicated to improving and saving lives. Competitive paid time off plus eight paid holidays. Community engagement and green initiatives. Medical, dental, and vision benefits effective on the first day of employment. Tuition reimbursement program. 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 produc…

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