Equal Opportunity Employer
Wednesday to Saturday Shift
Purpose of Position:
The position involves the performing of routine and non-routine analyses of raw materials, in-process materials and finished products in accordance with cGMP guidelines. The appropriately trained individual may provide training and guidance to other QC Analysts. The individual troubleshoots problems associated with methods and instruments resolving them where possible or seeking guidance/authorization where required.Key Responsibilities:⦁ Understands importance and priority of EHS and takes personal responsibility for their own safety; looks out for the safety of colleagues and avoidance of all incidents; willingly engages in and embraces activities to improve EHS performance in the working environment.⦁ Test and analyze samples in a timely manner in support of project plans in accordance to cGMP guidelines⦁ Review analytical data for compliance with specifications and cGMP guidelines⦁ Assist in development of experimental procedures and protocols⦁ Develop/revise documentation such as SOP, testing procedures and material specifications⦁ Provide training and guidance to other analystsJob Knowledge Required:⦁ BS in chemistry, biology or related discipline⦁ 2-5 years experience as a QC analyst/chemist in a GMP environment preferred⦁ Experience and familiarity with analytical testing equipment and methodology including HPLC, Karl Fischer, Spectrophotometry (UV/VIS, IR, NMR), and possibly LCMS.Problem Solving:The individual must resolve complex non-routine problems requiring in-depth evaluation of data/factors. The position may determine appropriate methods and procedures for new assignments.Accountability:The position is accountable to ensure that analytical work meets agreed schedules while fully complying with cGMP procedures and regulations.