Catalent Pharma Solutions

pharmaceutical

MS&TCoordinator

Kansas City, Missouri, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“MS&T Coordinator at Catalent Pharma Solutions. Skills: process management, coordination, stakeholder management. Coordinate projects ensuring correct technical requirements documentation generated. Monitor technical requirements documentation adherence and completion”

Industry & Context.

pharmaceutical
Problems you'll solve

Root cause analysis

Eligibility Requirements

100% based on-site in Kansas City

What They're Looking For.

Must Have

Bachelor's Degree in Engineering, Science or equivalent work experience required, 2+ years of experience with GMP equipment/manufacturing/healthcare/pharmaceutical, 2+ years of experience in a customer service or appropriate business-related area, Good knowledge of manufacturing equipment and GMP processes, Good Time Management/Organizational skills adopting a committed approach to providing a high level of customer service when managing multiple tasks, A good working knowledge of Microsoft Office Word, PowerPoint, Excel and Visio, The ability to work as part of a team, adopting the right first-time approach ensuring the commitments are met in a timely manner, Demonstrated professionalism including excellent work ethic, positive attitude and experience communicating with external clients

Nice to Have

Artios CAD experience

What You'll Do.

Coordinate projects ensuring correct technical requirements documentation generated

Monitor technical requirements documentation adherence and completion

Attend and produce minutes and actions for internal client meetings

Understand full scope requirements to generate project documentation

Provide information to MS&T on specific project requirements

Deputize specific tasks in the MS&T’s absence

Assist with departmental training and completion of training documentation

Assist in preparation and review of Standing Operating Procedures

Support Complaint & Deviation investigations

Support root cause analysis

Stay appraised of development within healthcare packaging industry

Perform any role/level within the CSE team if trained

How You'll Work.

Team & Collaboration

Work with clients through Manufacturing; Act as part of a MS&T team; Work as part of a team; Communicate with external clients

Communication Scope

Experience communicating with external clients

Process & Methodology

Coordinate projects, Ensure correct technical requirements documentation generated, Monitor technical requirements documentation adherence and completion, Generate required project requirements documentation

Full Job Description

**Manufacturing Sciences and Technology Coordinator** **Position Summary** * **Work Schedule: Monday to Friday 7am-4pm** * 100% based on-site in Kansas City ​**​** Catalent Pharma Solutions in Kansas City, MO is hiring an MS&T Coordinator. The Manufacturing Sciences and Technology (MS&T) team will lead technical process support for the Kansas City operations, including the development of the package and process with clients through Manufacturing. The team consists of strong engineers, scientists, designers or qualified people to be technology transfer process owner to deliver excellent services to internal and external customers. **The Role** * Under direction from MS&T team coordinate projects ensuring correct technical requirements documentation generated, monitored and assist to ensure successful adherence and completion. * Attend and produce minutes and actions for internal client meetings to support MS&T team and understand full scope requirements to generate required project requirements documentation. * When acting as part of a MS&T team, provide information to MS&T on specific project requirements and deputize specific tasks in the MS&T’s absence. * Assist with departmental training and completion of training documentation. * Assist in the preparation and regular review of Standing Operating Procedures relating to your own areas of responsibility. * Support Complaint & Deviation investigations and root cause analysis. * Stay appraised of development within the healthcare packaging industry. * Any other duties which may properly be assigned to this post. * May be requested to perform any role/level within the CSE team if trained to do so. * All other duties as assigned **The Candidate** * Bachelor’s Degree in Engineering, Science or equivalent work experience required * 2+ years of experience with GMP equipment/manufacturing/healthcare/pharmaceutical * 2+ years of experience in a customer service or appropriate business-related area * Good knowledge of manufa

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