Scientist-II, QC

Scientist-II, QC: Fairfield, NJ: Interpret, apply & ensure compliance w/ global regulatory reqrments, cGMP, GLP, & data integrity standards. Rqrmts: Mst hve Master’s deg. (or US equiv) in Pharmacy, Chem. or Pharma. Sci. & 3 yrs exp in pharma. quality envirnment. Hands-on exp w/ GxP dcumntation, chnge cntrol prcsses, artwrk rview, & preprtion of quality doc., incldng SOPs, STPs, spcfctions, & vendor qulfction materials. Exp. w/ reg. audits, compliance doc., & strong understanding of product release & quality lifecycle is req. Must possess thorough knowledge of reg. reqirments, strong comm. skills, & proficiency in MS & tech. writing. 40 hrs/wk, 9:00 - 5:00 p.m. Must hve proof of legal authority to work in the U.S.