Not specified; not specified; comprehensive medica...
Not specified
Review executed batch production records
Ensure adherence to cgmp standards
Verify documentation against master records
Lonza Group is seeking a Batch Record Reviewer in Tampa, FL, to ensure the accuracy and compliance of manufacturing documentation in a fast-paced biopharmaceutical environment. The ideal candidate will possess at least 2 years of experience in a cGMP-regulated setting, with strong analytical skills and attention to detail
Job Summary
This role ensures the accuracy and compliance of critical manufacturing documentation that supports timely product release.
The position offers an agile career within a dynamic Quality organization built on collaboration and integrity.
Candidates will partner with Manufacturing, QC, QA, MSAT, and Supply Chain to resolve documentation gaps.
Matching Summary
Match Score: 85
Lonza Group is seeking a Batch Record Reviewer in Tampa, FL, to ensure the accuracy and compliance of manufacturing documentation in a fast-paced biopharmaceutical environment. The ideal candidate will possess at least 2 years of experience in a cGMP-regulated setting, with strong analytical skills and attention to detail.
Salary
Not specified; Not specified; Comprehensive medical, dental, and vision insurance included
Skills & Requirements
Must-have
Review executed Batch Production Records
Ensure adherence to cGMP standards
Verify documentation against master records
Confirm critical process parameters
Strong attention to detail
Nice-to-have
Experience with QMS systems
Proficiency in SAP or TrackWise
Support continuous improvement initiatives
Collaborative team environment
Clear communication of findings
Key Requirements
High school diploma required
2+ years experience in pharmaceutical manufacturing or QA