Review daily instrument calibration and verifications; and review of logbooks

　　Review testing with other analysts and supervisor

　　Perform calibration and system suitability using approved Methods

　　Problem solve with colleagues regarding OOS results, discuss additional testing, operation of equipment, meeting to share ideas. CAPA responsibility

　　Review NCRs prior to submission to Lab Manager, check calculations, possible cause with review of batch records.

　　Assist with quality and environmental health and safety audits

　　Perform analytical testing using HPLC, GC, ICP-OES, UV-VIS, Karl Fischer, etc.

　　Compliance to Data Integrity requirements

　　Assist with investigation of quality issues such Out of Specification (OOS), Out of Trends (OOT), etc.

　　Train on and support the chemical hygiene program for the laboratory

　　Execute testing methods, protocols and other work instructions

　　Assist in managing of chemical and consumable stocks

　　Perform calibrations and system suitability under supervision

　　Familiar with USP/NF Compendia, ASTM, ISO Stds

　　Familiarity with US FDA 21CFR Part 210 & 211 (Drug Product) and Cosmetic GMPs

　　Requirements

　　Bachelor’s degree in Chemistry or related field

　　Strong knowledge in GMP, GLP, Root Cause Analysis & Corrective Action Planning Tools

　　Laboratory management experience preferred, with experience in Cosmetic or Pharmaceuticals desired

　　1+ years Quality Control Analytical Lab experience with HPLC, GC, ICP-OES, UV-VIS, Karl Fischer, etc

　　Good interpersonal and written communication

　　Flexible, ability to multitask and designate

　　Good organizational skills

　　Benefits

　　Medical, Dental, and Vision Insurance

　　Life Insurance paid 100% by the company

　　401K after 6 months