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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.
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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
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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.
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