Assistant General Manager

0 years

0 Lacs

Posted:2 days ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

  • Literature search by Sci-Finder and evaluation, summary of literature search and finalization of ROS base on cheaper and commercially available raw materials.
  • Check and define the feasibility of proposed ROS, design the experiments and optimization of process
  • Handle CIP-project to ensure shortest process, best recovery and minimum RMC.
  • Responsible to resolve any issues/queries related to other departments such as QA, RA, Analytical, PE and Plant w.r.t. product process, scale-up, technology transfer, risk assessment, investigation of any failure, etc.
  • Evaluation of GTI and N-nitroso impurities in drug substance.
  • To develop cost effective process meeting regulatory quality and minimum environmental hazardous process by following cGMP & GLP guidelines.
  • Provide support to the subordinates to achieve the goal by using technical knowledge and experience.
  • Characterization of working standards of KSM, intermediates and finished products and impurity standard by using PXRD, 1H NMR, 13C NMR, IR, Mass, DSC, TGA and ICP-MS techniques.
  • Create novel ideas and implement them to create IP assets after discussion with IPR team and superior. (Patent filling)
  • Preparation of technical package for customers and process development report (PDR) and reviewed the documents.
  • Training and development of the team members.
  • Lab maintenance and ensure that all equipment used in the lab are calibrated, validated, clean and in good condition.

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Cadila Pharmaceuticals Limited logo
Cadila Pharmaceuticals Limited

Pharmaceuticals

Ahmedabad

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