Research experience, knowledge in extraction and isolation techniques chromatography purification, HPLC, etc and characterization of natural products and their modifications. M.Sc, M.S. in Chemistry, Organic Chemistry, Natural Products Chemistry, Medicinal Chemistry, Pharmaceutical Chemistry from a recognized university or equivalent.

Evaluates new market complaints daily and communicates them to the various manufacturing partners, determines the criticality of complaints and makes appropriate recommendations. Escalates critical complaints and those with the potential to affect an entire batch or multiple batches. 

This is a non-supervisory position in Reference Standard Laboratory responsible for performing the required tests as part of the project and maintaining the GLP environment in the Laboratory. The incumbent will utilize his or her technical expertise, knowledge of pharmaceutical analysis in collaborative testing, efficient and effective laboratory operations.

Support affiliates in updating local requirements based on regulatory agencies guidance and input from affiliates, distributors. Manage working relationships with key stakeholders. Ensure compliance with regulatory requirements and provide strategic product direction to teams.

Lupin Healthcare Limited, the wholly owned subsidiary of global pharma major Lupin Limited announced today the acquisition of Renascience Pharma Limited , a UK-based pharmaceutical company and sole supplier of 4 specialty products targeting unmet medical needs in the UK.

B.Pharma OR D. Pharma with minimum of 6 years of experience in procurement of drugs and other pharmaceutical, medical products, relevant experience in public sector, private sector, any reputed organization OR M. Pharma with minimum of 2 years of experience in procurement of drugs and other pharmaceutical, medical products, relevant experience.

Teaching and Research work. M.Pharm, Ph.D preferred. Ph.D mandatory for Professor.

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.

Person should be well experienced in Environment Monitoring of Injcetable facility Settle plate, air sampling, surface monitoring and personnel gown monitoring. He must be aware of good documentation practices and aseptic behavior.

R&D Data Steward plays a critical role in the intersection between business and data, where stewards will guide business teams on how to unlock value from data. This role will drive definition and documentation of R&D data standards in line with enterprise.