Qa Documentation Specialist

Catalent

St. Petersburg, FL, US
Competitive pyy; day-one benefits; 152 hours pto +...
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Bachelor's degree in business or science
3 years experience with documentation systems
1 year pharmaceutical industry experience
** Catalent is seeking a Quality Assurance Documentation Specialist for its St. Petersburg, FL facility. This on-site role involves managing quality documentation and electronic systems, requiring a background in documentation systems and experience in the pharmaceutical industry. **

Job Summary

  • This position is 100% on-site at the St. Petersburg facility, which has a capacity of 18 billion capsules per year.
  • The role involves reviewing, issuing, and closing Document Change Requests while maintaining quality documents in systems like Documentum.
  • Candidates will manage standard operating procedures, batch records, and electronic system recipes in compliance with Catalent's SOPs.

Matching Summary

Match Score: 75

** Catalent is seeking a Quality Assurance Documentation Specialist for its St. Petersburg, FL facility. This on-site role involves managing quality documentation and electronic systems, requiring a background in documentation systems and experience in the pharmaceutical industry. **

Salary

Competitive pay; Day-one benefits; 152 hours PTO plus 8 paid holidays

Skills & Requirements

Must-have

  • Bachelor's degree in business or science
  • 3 years experience with documentation systems
  • 1 year pharmaceutical industry experience
  • 1 year experience authoring electronic batch record recipes
  • Understanding of cGMPs for documentation systems

Nice-to-have

  • Knowledge of Documentum computerized systems
  • Experience with LIMS and POMS applications
  • Familiarity with JDE and finished goods label generation
  • Ability to work under pressure with changing priorities

Key Requirements

  • Bachelor's degree required
  • Minimum 3 years documentation system experience
  • Minimum 1 year pharmaceutical industry background
  • Minimum 1 year electronic batch record recipe authoring
  • cGMP knowledge required

Work Rights

Not specified

Tailored Resume

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