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.
#J-18808-LjbffrSenior Consultant - Data Integrity and Sterility GMP in greenville at Unknown Company
This position is listed as full time and onsite.