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Supervisor, Production - Kansas City Missouri
Company: Disability Solutions Location: Kansas City, Missouri
Posted On: 01/19/2025
Supervisor, ProductionPosition Summary: 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.Catalent Pharma Solutions in Kansas City, MO is hiring a Supervisor, Production. The Production Supervisor will manage the day-to-day activities and employees within the Packaging Group.-- This individual will ensure that all work is carried out in accordance with regulatory requirements, Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOPs).-- This individual will constantly evaluate the internal processes and procedures and work to create an efficient packaging area while maintaining the highest possible quality.This is a full-time, salary role. ----This is onsite.-- This position is a 2nd shift role, Monday - Friday, 2:30pm - 11:00pm.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: - Responsible for process improvements, procedures and written content of those procedures
- Responsible for the management and development of direct reports
- Responsible for the quality, efficiency and timeliness of outputs
- Responsible for presenting and defending policies and procedures to both internal and external management and auditors
- Ability to obtain comprehensive knowledge of cGMPs and accepted industry standards
- Need to proactively investigate, evaluate and potentially implement the latest industry trends
- Ensure compliance with safety guidelines and proper operating parameters
- All other duties as assignedThe Candidate:
- High School diploma or General Education Degree is required
- Bachelor's degree is preferred
- Requires at least five years of relevant experience in Production Operation or previous scheduling roles
- Understanding of Pharmaceutical Manufacturing is required
- Experience in the contract Pharmaceutical industry preferred
- 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
- Intermediate computer skills - including, but not limited to e-mail, Microsoft Word, Microsoft Excel, Internet Explorer, Inventory systems, equipment Human/Machine Interface (HMI)
- Individual may be required to sit, stand, walk regularly and occasionally lift up to 50 poundsWhy You Should Join Catalent:
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