Clinical Coordinator

Catalent

Philadelphia, PA, US
Create batch records based on source documentation
Gmp standards compliance for packaging
Coordinate receiving and purchase order generation
The primary responsibilities include creating batch records based on project source documentation while ensuring adherence to GMP standards

Job Summary

  • The primary responsibilities include creating batch records based on project source documentation while ensuring adherence to GMP standards.
  • Catalent's facility serves as the global Center of Excellence for Clinical Supply Packaging, offering manual to fully automated solutions.
  • Employees benefit from 152 hours of PTO plus 8 paid holidays, generous 401K match, and tuition reimbursement opportunities.

Matching Summary

The primary responsibilities include creating batch records based on project source documentation while ensuring adherence to GMP standards.

Skills & Requirements

Must-have

  • Create batch records based on source documentation
  • GMP standards compliance for packaging
  • Coordinate receiving and purchase order generation
  • Interact with Production and Quality Assurance teams

Nice-to-have

  • Client interaction and question facilitation
  • Experience in clinical trial material distribution
  • Ability to work in a dynamic pace environment
  • Strong personal initiative and problem solving

Key Requirements

  • High School Diploma or GED required
  • Associate's or Bachelor's degree preferred
  • At least one year pharmaceutical environment experience preferred
  • GMP experience preferred
  • Previous packaging batch record preparation experience preferred

Work Rights

Not specified

Tailored Resume

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