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.
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This position is listed as full time and onsite.