​​​​Position: Executive - Analytical - Research & Development


 Location: Chennai     


 Job Code: TLS/AD/24 (Please mention the JOB CODE on the subject of the mail)


 Qualification: M. Pharm /M.Sc. Chemistry / B. Pharm

 (Eligible candidates can apply by sending an e-mail to hr@theragenlifesciences.com)


 Experience: 0 to 3 Years


 Job Location:Chennai


 Roles & Responsibility:

  • To Perform testing of raw materials and active pharmaceutical ingredients.

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  • To perform the testing of in-process and finished pharmaceutical goods.

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  • To prepare SOP’s.

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  • To Prepare protocols for studies.

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  • To perform method developments.

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  • To perform method validations.

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  • Liaise effectively with the cross functional team members to meet the timeline of the project.

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  • Prepare all necessary documentation for technology transfer of products and actively involve in the execution.

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  • Strictly adhere to in-house systems and procedures to ensure fulfils regulatory requirements

Theragen LifesciencesPVT LTD


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Theragen Lifesciences PVT LTD

Welcome to the career section of Theragen Lifesciences Pvt Ltd. We are a leading pharma research organization and encourage development of knowledge, skills and attitudes to enable our people to perform to their full potential. We believe in identifying top talented professionals from the industry as well as freshers from various university. We look forward to receiving your application!


WE ARE RECRUITING!!!

 ​Position: Executive - Formulation - Research & Development


 Location: Chennai     


 Job Code: TLS/FD/24 (Please mention the JOB CODE on the subject of the  mail)


 Qualification: M. Pharm (Pharmaceutics/Pharmaceutical Technology) 

 (Eligible candidates can apply by sending an e-mail to hr@theragenlifesciences.com)


 Experience:  0 to 3 Years


 Job Location:Chennai


 Roles & Responsibility:

  • To execute Pre-formulation studies, bench scale batches using different  formulation processes.


  • To support and execute the tech transfer activities, pilot batch  manufacturing and bioequivalence studies etc.


  • Coordination and correspondence for the arrangement of API, RLD, Excipients, Punches and other accessories for Lab scale batches.


  • Coordination with cross functional departments like RA, QA, QC and  AR&D.


  • Should have knowledge of Solid oral and liquid oral dosage form  development.


  • Should have good knowledge of F R&D equipment and their handling.


  • Responsible for conducting Literature search, Experimental batches, Pilot and Pivotal batches.


  • Should have exposure in patents and non-infringing development.


  • Must be able to prepare development documents like Master Formula  Records (MFR/MPR), development protocols, and pharmaceutical  development report.


  • Need to be develop the Products by QbD fashion and expertise in DoE  studies and interpretation using competent software.


  • Willingness and Cooperation to work at Contract Manufacturing  Organization (CMO) sites.​