QC Scientists
$83k - $87kOcimpharma
Job Responsibilities Conduct quality control chemical testing of raw materials, in-process, and finished pharmaceutical products using HPLC/UPLC, GC-HS, UV Spectrometry, physicochemical characterization, Particle size analysis, and in-vitro drug release testing; Prepare, review, and execute technical documentation, including Analytical methodologies, method verification, validation, and transfer protocols, and reports and SOPs; Perform investigations of out-of-specification (OOS) laboratory results using OOS/OOT, CAPA; Maintain laboratory record and interpret data using statistical principles; Maintain and troubleshoot analytical equipment and coordinate equipment qualification and calibration activities using AAS (Atomic Absorption Spectroscopy) and Dissolution. Requirements Require Master’s degree in Chemistry or Pharmaceutical Chemistry plus skills and knowledge in HPLC, GC, UV Spectrometry, Analytical Methodologies, Dissolution, Particle size analysis. Job location: Pine Brook, NJ. Standard benefits with $83k~$87k/year. #J-18808-Ljbffr Ocimpharma
Vacancy posted 22 hours ago
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