MS&T Project Coordinator - Pharma Packaging

Catalent; Kansas City (MO); On-site; USD 65,000 - 75,000; Full time

Job summary

Catalent is hiring a Coordinator, Manufacturing Sciences & Technology (MS&T) in Kansas City, MO. The role supports project delivery, technology transfer into packaging, and maintains cGMP-compliant documentation.

Typical hours are 7am-4pm, on-site, with cross-functional collaboration across packaging,analytical services, and clinical supply teams. Responsibilities include coordinating documentation, attending client meetings, and assisting with SOPs and training.

Qualifications

• Bachelor’s degree in Engineering, Science, or equivalent work experience.
• 2+ years of GMP equipment, manufacturing, healthcare, or pharmaceutical experience OR 2+ years in customer service or a related business area.
• Strong time management and organizational skills with a commitment to high-level customer service.
• Proficiency in Microsoft Word, PowerPoint, Excel, and Visio.

Responsibilities

• Coordinate projects under MS&T direction, ensuring documentation is generated, monitored, and completed.
• Attend internal client meetings, produce minutes and actions, and support MS&T in understanding full scope requirements.
• Provide project-specific information to MS&T and deputize tasks in their absence.
• Assist with departmental training and maintain training documentation.
• Prepare and review Standard Operating Procedures related to assigned responsibilities.
• Support complaint and deviation investigations and root cause analysis.
• Stay informed about developments in the healthcare packaging industry.
• Perform other duties as assigned, including roles within the CSE team if trained.

Skills

Project coordination

Communication skills

Customer service mindset

Team collaboration

Education

Bachelor's degree in Engineering/Science

Tools

Microsoft Word

PowerPoint

Excel

Visio

Artios CAD

Job description

Catalent is hiring a Coordinator, Manufacturing Sciences & Technology (MS&T) in Kansas City, MO. The role supports project delivery, technology transfer into packaging, and maintains cGMP-compliant documentation.

Typical hours are 7am-4pm, on-site, with cross-functional collaboration across packaging,analytical services, and clinical supply teams. Responsibilities include coordinating documentation, attending client meetings, and assisting with SOPs and training.