Quality Control Chemist II

Quality Control Chemist II - Release TeamThis role is located at our headquarters in North Augusta, South Carolina. Relocation is required. Primary Responsibilities:Use basic understanding and knowledge of techniques, instrumentation, and lab functions to identify problems and support the completion of work assignments.Hands on experience with HPLC/UPLC, GC, GC-MS, IC, KF and other routine analytical equipment such as pH meter and balance.Perform quality control routine critical testing for raw material/ Intermediate/ Release / Stability testing and evaluate stability trends.Ensure completion of all the testing release, stability and validation work in timely manner.Perform Method development and method validation execution, including writing protocols and reports. Must be proficient.Responsible for reviewing analytical laboratory raw data and electronic records.Assist the QC group with writing and editing of deviations, CAPA, OOS and OOT.Maintain the QC lab by ordering supplies routinely used for testing.Assist the QC/QA group with writing and editing of SOPs and STPs.Qualifications:Master’s Degree in Chemistry or life sciences with 1-2 years of experience in a GMP environment, or Bachelor’s degree in Chemistry or life sciences with 2-5 years of experience in a GMP environment.Hands-on experience with HPLC/UPLC, GC, GC-MS/LC-MS, KF, IC.Hands-on experience with Empower and/or Chemstation. Experience with MassLynx is desirable.Familiarity with both CFR 21 and ICH guidelines regarding GMP.Computer skills in MS Word, EXCEL, and Access.ADA-These Requirements are a Condition of Employment: Must be able to push, pull, squat, stand and walk through-out the dayMust be able to lift up to 50lbsMust be able to wear safety shoes & glasses through-out the day while in designated areas. (provided by the company)You must be cleared by a physician to wear a respirator throughout the day while in designated areas.Must be able work in a chemical environment.