Manager, Manufacturing Operations - 2nd 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 a Manager, Manufacturing Operations - 2nd shift to join our team. This role leads second-shift cGMP manufacturing at the Kansas City site, ensuring quality products are produced on time and in full compliance with safety and regulatory standards. The position oversees front-line Supervisors and their teams, driving performance in safety, quality, delivery, cost, and engagement. As the senior leader on site during the second shift, this role makes real-time operational decisions, fosters collaboration across departments, and builds leadership capability for future growth. Shift: M-Th 1:30pm-12am Location: Kansas City, MO 100% Onsite The Role Lead all second-shift manufacturing activities, ensuring schedule adherence, effective resource deployment, and achievement of daily production commitments. Serve as the senior operations decision-maker on shift; resolve workflow, processing, equipment, and utility issues and escalate significant risks promptly. Ensure disciplined shift-to-shift handoff, communication, and continuity of open issues, deviations, and priorities. Support 24/7 operations, including flexibility for coverage across shifts and weekends as business needs require. Ensure compliance with all cGMP, OSHA, environmental, and Catalent safety standards; proactively identify and correct unsafe conditions and behaviors. Ensure Supervisors and operators are trained and executing to approved operating and cleaning procedures and applicable regulations. Ensure batch records are complete, accurate, and right first time. Define and execute corrective and preventive actions in response to deviations and internal, regulatory, and client audit findings; meet commitments on time. Maintain the facility in a tour-ready state at all times; support regulatory agency and client audits and on-site visits. Manage and develop front-line Supervisors and their teams, including selection, onboarding, performance evaluation, coaching, and discipline. Build supervisory capability and succession depth; identify high-potential talent and create development plans for growth. Partner with Human Resources on recruitment, retention, training, engagement, and workforce planning. Foster an inclusive, accountable environment where associates are encouraged to speak up and contribute improvement ideas. Track, analyze, and report shift performance metrics; identify trends and drive corrective actions. Lead Lean and continuous improvement initiatives to improve throughput, right-first-time performance, and cost efficiency. Partner with Supply Chain, Quality Assurance, Engineering, Facilities, and other support groups to ensure smooth operations and resolve constraints. Support technology transfers, new product introductions, equipment commissioning, and validation activities executed on shift. Perform other duties and responsibilities as assigned. The Candidate Minimum Requirements Bachelor’s degree in Engineering, Pharmaceutical Sciences, Chemistry, Biology, Business, or a related discipline required; equivalent combination of education and progressive manufacturing leadership experience will be considered. Demonstrated experience leading front-line supervisors or comparable people leaders. Minimum of 7 years of experience in pharmaceutical, biotechnology, CDMO, or another highly regulated manufacturing environment, including at least 3 years leading people. Working knowledge of cGMP requirements, batch record execution, deviation and Corrective and Preventive Action (CAPA) systems, and the partnership between Operations and Quality. Strong operational problem-solving and decision-making skills, including the ability to make sound judgments independently during off-shift hours. Demonstrated capability in Lean manufacturing, structured problem …

View the full posting and apply