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Senior QC Chemist - Pharma

Biocon - Cranbury, NJ

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Job Description

Job Purpose:Perform routine testing and decides on the acceptability of the in-process, process validation samples, raw materials, packaging materials, finished products, stability samples and developmental samples in a regulated laboratory environment.Analyze and interpret results in written and oral format.Duties and ResponsibilitiesPerform routine tests of Raw materials, Packaging materials, In-process and Finished products and stability samples including wet chemistry analysis, dissolution, content uniformity, assay, particle size distribution, density, water determination by KF, and other tests according to the in-house monographs and USP using classical wet chemistry and instrumental (HPLC, GC, etc).Evaluates test results and decides acceptability of the samples based on the test results.Maintain accurate lab notebooks and complete all related analytical reports, write summaries, and keep proper documentation in compliance with SOPs.Maintain the laboratories with good housekeeping practices and in compliant with cGMP.Ensure notebooks are reviewed in a timely manner, in accordance with SOPs.Writes or revise test procedures, protocols, SOPs, based on the outcome of the experimental design.Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment and Safety PracticesEducationand/or Experience:Bachelor's degree in Chemistry or Pharmacy or related scientific field with minimum 4 to 8 years' experience in Pharmaceutical analysis or Master's degree in Chemistry or Pharmacy or related scientific field with minimum 4 to 8 years' experience in Pharmaceutical analysis.Clear understanding of normal, molar and percent concentrations. Ability to prepare solutions according to a required concentration.Ability to deal with problems involving several concrete variables in standardized situations.Must have Valid work permit.

Created: 2025-10-01

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