Qa Specialist, Operations - Warehouse

Lonza Group

Tampa, FL, US
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Cgmp regulated pharmaceutical environment experience
Sop and batch record review skills
Deviation assessment and root cause investigation
** Lonza Group is seeking a QA Specialist for their Operations team in Tampa, FL, to ensure GMP compliance and support the quality assurance of manufacturing operations. The ideal candidate will have experience in a cGMP-regulated environment and strong documentation and collaboration skills. **

Job Summary

  • This role plays a critical part in supporting GMP compliance, documentation accuracy, and audit readiness across manufacturing operations.
  • The position involves reviewing SOPs, batch records, and test methods to ensure all activities are documented accurately according to procedures.
  • Candidates will support internal, vendor, and customer audits while collaborating with cross-functional teams to troubleshoot quality issues.

Matching Summary

Match Score: 75

** Lonza Group is seeking a QA Specialist for their Operations team in Tampa, FL, to ensure GMP compliance and support the quality assurance of manufacturing operations. The ideal candidate will have experience in a cGMP-regulated environment and strong documentation and collaboration skills. **

Skills & Requirements

Must-have

  • cGMP regulated pharmaceutical environment experience
  • SOP and batch record review skills
  • Deviation assessment and root cause investigation

Nice-to-have

  • Track Wise and SAP software familiarity
  • Microsoft Office proficiency
  • Continuous improvement mindset

Key Requirements

  • High school diploma required
  • Bachelor's degree preferred
  • 3 years of relevant work experience

Work Rights

Not specified

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