April 2025

Pass in D.Pharma, B.Pharma or Intermediate vocational course in Pharmacy recognized by Government. Must be registered with the Pharmacy Council. In case of candidate possess both D.Pharma and B.Pharma, the maximum percentage secured in any of the above shall be considered.

Post-Graduation in Science M.Pharm, Life Sciences, Biotech, Zoology, Botany etc, with PG Diploma in Clinical Research is Mandatory. Experience Desirable, in handling multicenter projects.

M.Sc, M.Tech, M.Pharm, B.Tech, B.Pharm. or equivalent in Biotechnology and allied areas with a minimum of 55% marks in the preceding qualification.

Masters, Integrated Masters in Natural or Agricultural or Pharmaceutical Sciences MVSc, Animal Sciences. OR Bachelors degree in Engineering or Technology or Medicine from a recognized University or equivalent. AND 2 years experience in Research and Development in Industrial and Academic Institutions or Science and Technology Organizations and Scientific activities and services.

Masters degree in Life Sciences or associated fields with National Eligibility Test qualification, with a minimum of 60% marks or equivalent grade. Research experience and practical knowledge of working with laboratory rodent models is required. Knowledge of basic molecular biology techniques including PCR is required.

Amneal Pharmaceuticals, Inc. is a global pharmaceutical company. Our team of 7,500+ colleagues helps make healthy possible through the development, manufacturing, and distribution of a diverse portfolio of 270+ high-quality medicines.

Should be able to develop analytical methods and perform analysis on UV, Dissolution, HPLC and ICP-OES instruments. Dissolution development, Comparative dissolution profile and multimedia dissolution study.

B.Pharm/M.Pharm/B.Sc/M.Sc; Production and Packaging, Planning, Monitoring and Reporting production activities. Purchase and procurement planning, monitoring and reporting purchase activities

Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors strategically important clinical-regulatory documents that are label focused and align with project strategies, regulatory requirements, and communications best-practices.