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Pharmaceutical manufacturing company (Ewing, NJ) seeks QC Chemist to perform new analytical method development, method validation & method verification for pharmaceutical raw materials and finished products. Perform OOS, OOT, GLP, GDP for analytical instruments like HPLC, GC, Ion Chromatography, ICP-MS. Review laboratory deviations such as gap analysis, CAPA. Create & review protocols for stability testing and method validation; write & review SOPs, reports for method validation & verification, and Stability testing protocols.  

Mail resume to: HR Dept., Navinta LLC, 1499 Lower Ferry Rd., Ewing, NJ 08618.

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