Returns Associate Ii

Catalent

Kansas City, MO, US
Follow safety and manual handling guidelines
Process returned clinical trial medications
Complete documentation in compliance with cgmp
The position supports clinical trial projects by processing returned medications for destruction while ensuring strict adherence to regulatory requirements and good manufacturing practices

Job Summary

  • The position supports clinical trial projects by processing returned medications for destruction while ensuring strict adherence to regulatory requirements and good manufacturing practices.
  • Employees will follow specific SOPs and destruction plans to handle materials safely and reconcile inventory within the Kansas City facility.
  • Catalent offers a defined career path, 152 hours of PTO plus 8 paid holidays, and tuition reimbursement for employees dedicated to advancing life-saving medicines.

Matching Summary

The position supports clinical trial projects by processing returned medications for destruction while ensuring strict adherence to regulatory requirements and good manufacturing practices.

Skills & Requirements

Must-have

  • Follow safety and manual handling guidelines
  • Process returned clinical trial medications
  • Complete documentation in compliance with cGMP
  • Reconcile returned material to inventory system
  • Meet daily targeted productivity goals

Nice-to-have

  • Ability to work in a team environment
  • Self-motivated and proactive approach
  • Proven written and verbal communication skills
  • High attention to detail
  • Basic computer skills including Excel

Key Requirements

  • High School degree or equivalent
  • 1-3 years of clinical trial returns or pharmaceutical operations experience preferred

Work Rights

Not specified

Tailored Resume

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