Employer requires a Masters degree in Regulatory Affairs for Drugs, Biologics, and Medical Devices, Biotechnology, Biochemistry, Pharmaceutical Science or a related life sciences field plus 24 months in Job offered, Quality Assurance Sr. Specialist, Quality Assurance Supervisor, Quality Assurance Lead, or related occupation. Experience must include 1 Pharmaceutical batch manufacturing record review, 2 Major deviation investigation handling, 3 Change control assessment, 4 TrackWise QMS Software, 5 Oracle Process Manufacturing OPM software, and 6 Inspection and Audit Management.
Categories: eb3
0 Comments