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Job description
United Pharma in Greenville, NC seeks experienced Senior Consultants to support a pharmaceutical client, focusing on retrospective Data Integrity review, Sterility Assurance, and GMP Quality within sterile products manufacturing.
Responsibilities include reviewing GMP documentation, ALCOA+, FDA 483 remediation, deviations and CAPAs; documenting findings in inspection-ready format and supporting investigations.
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Worksite address
greenville, NC, 27834, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.