Newark Metro Area, NJ
Responsible for management of non GMP development stability facility for Analytical Development .
The candidate will manage sample pull and protocol in stability LIMS, sample inventory, and ensure EHS compliance of the lab. May support GMP stability area as necessary. Will report to Director Analytical Development.
BS/MS/Chemistry or relevant discipline with equivalent experience. Ph.D. Chemistry candidates will be considered.
Minimum 2 - 4 years recent cGMP/GLP pharmaceutical laboratory experience.
Prior stability experience is required.