GMP QC Chemist

Please note this is a 6 month contract position.The client wants candidates who have a good understanding of GMP and is able to explain it well. The location is Titusville, NJ. Schedule: Hours/Schedule: 40hrs/week / 8am-5pm (M-F)The Associate Analyst QC conducts analytical testing of stability samples submitted to the QC laboratories according to testing schedules in a productive and efficient manner.This position requires testing to be completed in compliance with all applicable procedures, standards and GMP regulations as well as all local, state, federal and international regulations and guidelines (FDA, EPA, DEA, OSHA, etc.)Requires a BA degree in the scientific field and 2-4 years exp.HM requests someone who can proficiently operate analytical instruments such as UPLC/HPLC, Dissolution, KFExperience working in a cGMP or GLP regulated environment. Performs routine analysis following methods and SOPs in a timely manner. Performs routine troubleshooting of laboratory instrumentsTop 3, non-negotiable skills: General knowledge of Chemistry and routine and non-routine testing methods and methodologies required. Strong attention to details, Communication and basic organization and time management skills are required.Applicants must provide their phone number. Job reference number A1209.