Group Lead

19 hours ago


Hyderabad, Telangana, India Sai Life Sciences Ltd Full time ₹ 6,00,000 - ₹ 18,00,000 per year
  • Ensure the good organization and housekeeping of the PRD department work area.
  • Plan and supervise developmental synthesis of the NCEs / API intermediate / target molecules.
  • Excel in the observation, recordings and reporting skill sets for the scientific data.
  • Work as a team and take responsibility with accountability.
  • Surveys the literature for information concerning specific compounds.
  • The Feasibility study of custom products involves close monitoring / supervision by research associate.
  • The Process Optimization shall be made on the selected route based on due diligence and literature during the feasibility studies.
  • Prior to designing laboratory experiments for process optimization, the MSDS of all input materials shall be obtained and scrutinized for risk assessment.
  • To improve processes for existing products and improve efficiency in cycle time.
  • Ensure and sign off the experimental data related to process development studies of the NCEs / API intermediate / target molecules manufacturing are recorded in Electronic Note Book (ELN).
  • To write process descriptions in the Technical Package and transfer optimized manufacturing strategies to production.
  • PRD to support the technology transfer team towards the efficient scalability of a given process to the manufacturing site.
  • To evaluate, recommend new technologies and equipment for synthesis, purification and implement their use in PRD and demonstrate the same to TT.
  • To support the clients with respect to all the analytical and CMC needs for each project being handled by PRD.
  • Actively participate in investigation of various complaints and quality related issues like CAPA, closing out the deviations in the manufacturing.
  • Ensure the good organization and housekeeping of the PRD department work area.
  • Plan and supervise developmental synthesis of the NCEs / API intermediate / target molecules.
  • Excel in the observation, recordings and reporting skill sets for the scientific data.
  • Work as a team and take responsibility with accountability.
  • Surveys the literature for information concerning specific compounds.
  • The Feasibility study of custom products involves close monitoring / supervision by research associate.
  • The Process Optimization shall be made on the selected route based on due diligence and literature during the feasibility studies.
  • Prior to designing laboratory experiments for process optimization, the MSDS of all input materials shall be obtained and scrutinized for risk assessment.
  • To improve processes for existing products and improve efficiency in cycle time.
  • Ensure and sign off the experimental data related to process development studies of the NCEs / API intermediate / target molecules manufacturing are recorded in Electronic Note Book (ELN).
  • To write process descriptions in the Technical Package and transfer optimized manufacturing strategies to production.
  • PRD to support the technology transfer team towards the efficient scalability of a given process to the manufacturing site.
  • To evaluate, recommend new technologies and equipment for synthesis, purification and implement their use in PRD and demonstrate the same to TT.
  • To support the clients with respect to all the analytical and CMC needs for each project being handled by PRD.
  • Actively participate in investigation of various complaints and quality related issues like CAPA, closing out the deviations in the manufacturing.

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