Associate Ii, Quality Assurance

Catalent

Kansas City, MO, US
High school diploma or ged
1-3 years packaging experience
Knowledge of cgmp and sops
The role supports clinical trial projects ensuring all work is performed in compliance with regulatory requirements and good manufacturing practices

Job Summary

  • The role supports clinical trial projects ensuring all work is performed in compliance with regulatory requirements and good manufacturing practices.
  • Responsibilities include creating Certificates of Analysis, inspecting bulk and finished products, and executing cleaning procedures.
  • Catalent offers a defined career path, 152 hours of PTO plus 8 paid holidays, and tuition reimbursement for degree completion.

Matching Summary

The role supports clinical trial projects ensuring all work is performed in compliance with regulatory requirements and good manufacturing practices.

Skills & Requirements

Must-have

  • High School diploma or GED
  • 1-3 years packaging experience
  • Knowledge of cGMP and SOPs
  • Proficiency in JD Edwards (IMS)
  • Ability to interpret specifications

Nice-to-have

  • Proactive problem-solving attitude
  • Mathematical and scientific reasoning
  • Computer technology skills
  • Dynamic fast-paced environment

Key Requirements

  • High School diploma or GED required
  • 1-3 years packaging experience preferred
  • Must follow written and oral instructions

Work Rights

Not specified

Tailored Resume

Cover Letter