Clinical Coordinator

Catalent

Philadelphia, Pennsylvania, United States
Create batch records based on source documentation
Prepare batch records following gmp standards
Generate zero-dollar purchase orders
The primary responsibilities include creating batch records based on source documentation while identifying customer needs and preparing records following GMP standards

Job Summary

  • The primary responsibilities include creating batch records based on source documentation while identifying customer needs and preparing records following GMP standards.
  • Catalent's Philadelphia-area facility serves as the global Center of Excellence for Clinical Supply Packaging, offering manual to fully automated solutions.
  • Employees receive 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 source documentation while identifying customer needs and preparing records following GMP standards.

Skills & Requirements

Must-have

  • Create batch records based on source documentation
  • Prepare batch records following GMP standards
  • Generate zero-dollar purchase orders
  • Interact with production and quality assurance teams

Nice-to-have

  • Experience in pharmaceutical environment preferred
  • Previous packaging and labeling experience
  • Ability to work in dynamic pace
  • Strong personal initiative and client interaction skills

Key Requirements

  • High School Diploma or GED required
  • Associate's or Bachelor's degree preferred
  • At least one year of pharmaceutical experience preferred
  • GMP experience preferred

Work Rights

Not specified

Tailored Resume

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