Quality Control Chemist

Job Title: QC ChemistLocation: New Jersey(Onsite)Duration: 6+ Months (Contract)only W2/1099Job SummaryOur client is seeking a hands-on QC Chemist to support quality control testing of raw materials, in-process/intermediate samples, and finished pharmaceutical products in a cGMP-regulated environment. This role involves routine analytical testing, data review, and compliance support within a fast-paced pharmaceutical QC laboratory.Key ResponsibilitiesPerform analytical testing of raw materials, intermediates, and finished products in compliance with cGMP requirementsExecute testing using analytical techniques including HPLC, GC (Headspace), FTIR, UV, and Ion Chromatography (IC)Conduct sample preparation, analysis, documentation, and review of analytical dataSupport method validation, method transfer, and troubleshooting activitiesPerform routine instrument operation, calibration, and maintenanceParticipate in deviation investigations, OOS/OOT investigations, and CAPA activitiesSupport internal and external audits and regulatory inspectionsMaintain accurate laboratory documentation in accordance with SOPs and data integrity standardsRole-Specific FocusQC Chemist IIStrong hands-on experience with GC Headspace and/or HPLCCapable of independent analysis, data review, and problem-solvingSupports method validation and technical troubleshootingQC Chemist IFocus on wet chemistry techniques, including:TitrationsKarl Fischer (KF) / KCL testingSolution and reagent preparationEquipment cleaning verification and swab testingWorks under established SOPs with supervision as neededRequired QualificationsB.S. in Chemistry or a related scientific discipline0–5 years of QC or analytical laboratory experience in the pharmaceutical industryWorking knowledge of cGMP regulations and QC laboratory practicesStrong attention to detail, documentation skills, and data integrity mindsetAbility to work independently and collaboratively in a fast-paced lab environment