vacancies

Post Graduation in Life- Science with PG Diploma in Clinical Research is Mandatory. Experience as Clinical research Mandatory.

Execution of technology transfer to Sun/CMO Site transfer, Scale up, Exhibit, Process validation batches plan

Experience in Regulatory Affairs, CMC, Manufacturing, Quality Assurance/Control, Process Development, or Analytical Development in the pharmaceutical or biotechnology industry

B.Pharm / M.Pharm; Archival and life cycle management of the CTD, e-CTD submission. Senior Executive Regulatory Publishing eCTD

M.Pharm, B.Pharm, M.Sc ; Analysis and sampling of the drug products, Drug substances, excipients, and water sample.

BPharm, MPharm, Pharm D, or MSc. Regulatory Affairs and Submissions Management.

Masters/ Integrated Masters in Natural or Agricultural or Pharmaceutical Sciences, MVSc, Animal Sciences. Or Bachelor s degree in Engineering or Technology or Medicine from a recognized University or equivalent.

M.Sc Bioinformatics, Biophysics, Biochemistry, Biotechnology or Masters degree in any other stream of Biological , Physical, Computational Sciences or Bachelors degree in Engineering or Technology or Medicine or Equivalent. Must have qualified GATE or NET-JRF or equivalent national level fellowship examination for JRF position.

B.Pharm with experience in Oral Liquid manufacturing. Should have good knowledge of documentation and qualification activities. Liquid Approved is desirable.