Piper Companies is seeking two GMP Manufacturing Documentation Consultants to join a 12-month, on-site engagement in Ridgefield, NJ. The role centers on authoring and maintaining Master Batch Records (MBRs) and other GMP documentation for a sterile injectable program.
Ideal candidates have hands-on MBR experience in aseptic/pharmaceutical environments, solid knowledge of cGMP/GDP/ALCOA+ data integrity, and advanced MS Word skills. Onsite work Monday through Friday with DOE pay rates.
#J-18808-LjbffrOnsite GMP Doc Specialist - Master Batch Records in ridgefield at Unknown Company
This position is listed as full time and onsite.