Quality Control Analyst - Stability Co-Ordinator
Newark Metro Area, NJ
Responsible for management of non GMP development stability facility for Analytical Development at Celgene Summit West site. 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. Manager open to Ph.D. Chemistry candidates.
Minimum 2 - 4 years recent cGMP/GLP pharmaceutical laboratory experience.
Prior stability experience is required.
Good communication skills.
Able to work well in team environment to achieve results.
Exhibits sound scientific judgment based on reasonable assumptions and available information.