Quality Assurance Manager: identify and write Standard Operating Procedures(SOP) to support quality assurance activities related to pharmaceutical manufacturing and distribution; track all investigations, Corrective and Preventive Action (CAPA), change controls and complaints.

Initiate CAPAs to identify and address adverse trends; prepare monthly, quarterly and yearly trend analysis reports; collect necessary data and prepare reports for Quality Review Board (QRB), Annual Product Review (APR) and quality control; interpret and analyze trend report data using statistical tools; perform quality audits; review and approve change controls, processes and analytical validation protocols, specifications, analytical methods and master batch records; perform statistical analysis of data; and coordinate regulatory and third party audits. 

Requires MS in in pharmaceutical management plus one year’s experience.

Location:  East Brunswick, New Jersey

Mail resumes to Casper Pharma, LLC- 2 Tower Center Blvd., Suite 1101C, East Brunswick, New Jersey 08816