Position Details
About this role
This role involves managing quality events, investigating discrepancies, and ensuring compliance within a pharmaceutical manufacturing environment, primarily on-site in St. Petersburg, FL.
Key Responsibilities
- Manage and document events/discrepancies
- Lead investigations and root cause analysis
- Prepare complaint investigation reports
- Track CAPA program effectiveness
- Ensure compliance with GMP and SOPs
Technical Overview
The position requires knowledge of cGMPs, OSHA regulations, investigation documentation, and quality systems in pharmaceutical manufacturing.
Ideal Candidate
The ideal candidate is a mid-level QA professional with at least three years of experience in pharmaceutical manufacturing, proficient in cGMPs, investigation writing, and root cause analysis, capable of managing discrepancies and ensuring compliance.
Must-Have Skills
Nice-to-Have Skills
Tools & Platforms
Required Skills
Hard Skills
Soft Skills
Industry & Role
Clearance & Visa
Keywords for Your Resume
Deal Breakers
Lack of experience in pharmaceutical QA, No knowledge of cGMPs or OSHA regulations, Inability to write investigations or perform root cause analysis, No relevant science degree, Unwillingness to work on-site
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