Catalent
pharmaceutical
ManufacturingSupportTeamCoordinator
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Manufacturing Support Team Coordinator at Catalent. Skills: process management, cross-functional coordination, vendor/stakeholder management, operational metrics, resource planning, continuous improvement. Coordinating and scheduling required training topics. Maintaining employee training files”
Industry & Context.
Ability to wear a PAPR (Powered Air Purifying Respirator) during manufacturing when required, Ability to wear required gowning required to work in the GMP manufacturing areas, Follows all Catalent safety procedures and identifies/communicates the necessary adjustments to address potential safety concerns, Will also ensure the proper use of PPE (Personal Protection Equipment)
What They're Looking For.
Must Have
Two years of progressive office experience, Computer literate and proficient in programs such as Microsoft Word, Microsoft Outlook, and Microsoft Excel, Thorough knowledge of cGMP, FDA, MHRA and DEA guidelines and how to apply them effectively
Nice to Have
Bachelor’s Degree or equivalent experience in the pharmaceutical industry, Thorough knowledge of Solid Dosage manufacturing
What You'll Do.
Coordinating and scheduling required training topics
Maintaining employee training files
Developing and maintaining department-specific training materials
Assisting with investigations
Continuous improvement projects
Manufacturing document generation & revision
Coordinates equipment training for Department employees including
and process training documentation
Works with Training department to maintain rosters in learning management system (ComplianceWire)
Maintain department-specific training materials including
and one-point lessons
Recommend changes and help build training material by collaborating with Pharmaceutical Manufacturing Leads and Operations Management
Assist in writing SOPs/SEPs for prosses and equipment used by pharmaceutics and operations personnel
Ensures 5S standards are met and maintained
Ensure that the facility is kept “tour ready” at all times and people/material/flow/cleaning and zone concepts are maintained at all times
How You'll Work.
Team & Collaboration
Collaborate with other site functions to identify and implement improvements to processes and procedures; Interact with employees at all levels inside and outside of the department as well as clients; Review documents with SME and Operations personnel
Communication Scope
Excellent written and verbal communications skills with internal and external customers
Process & Methodology
continuous improvement projects
Full Job Description
**Manufacturing Support Team Coordinator** **Position Summary** * **Work Schedule:** M-F 8am-4pm * **100% based on-site in Kansas City** 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. At the direction of the MST Manager, the **Manufacturing Support Team Coordinator** functions include coordinating and scheduling required training topics, maintaining employee training files, developing and maintaining department-specific training materials, assisting with investigations, continuous improvement projects and manufacturing document generation & revision. **The Role** * Coordinates equipment training for Department employees including, but not limited to, scheduling, assigning a trainer, and process training documentation. * Works with Training department to maintain rosters in learning management system (ComplianceWire). * Maintain department-specific training materials including, but not limited to, questionnaires, skill assessments, presentations, and one-point lessons. * Recommend changes and help build training material by collaborating with Pharmaceutical Manufacturing Leads and Operations Management. * Assist in writing SOPs/SEPs for prosses and equipment used by pharmaceutics and operations personnel. * Lead and collaborate with other site functions to identify and implement improvements to processes and procedures that simplify and improve efficiency while maintaining compliance with cGMPs and Catalent standards. * Must be able to interact with employees at all l
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