Job Location : Melville,NY, USA
Leading LI Mfr. of nutritional supplements seeks a hands-on entry to senior level QA Document Control Associate. Strong verbal & written skills required. Good organizational skills, Excellent oral and written communication skills, Computer literacy a must - Proficient in MS Suite (Word, Excel, Access, Power Point), Type 50 WPM or better a plus. Knowledge of GMP's, batch record review, and product release required. AS or BS degree in related sciences or 2 to 5 years experience in a GMP environment.