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.

Thorough understanding of Quality Control investigations, including Lab Incidents, OOS, and OOT. Relevant experience in Oral Solid Dosage formulations and / or Active Pharmaceutical Ingredient processes.

Granules India is a vertically integrated, high-growth pharmaceutical company with 38 years of proven performance and increasing performance and increasing presence across the world.

You will be embedded in our client's study team and have a dedicated ICON line manager to support you. Oversees all aspects of study site management to ensure high quality data resulting in consistently low query levels and in good Quality Assurance reports

Provide technology delivery leadership and domain expertise for Biological Studies product teams that enable in silico, in vitro and in vivo experimentation. Partner with Research and Technology leaders to create technology delivery strategy and prioritized agenda for Biological Studies.

Masters degree in pharmacy, life sciences, pharmaceutical management with relevant experience in the biopharma, healthcare, or market research sector is required.

U.S. Food and Drug Administration approval of a New Drug Application for KHINDIVI hydrocortisone Oral Solution as a replacement therapy in pediatric patients five years of age and older with adrenocortical insufficiency.

GSK plc announced that the US Food and Drug Administration (FDA) has approved Nucala (mepolizumab) as an add-on maintenance treatment for adult patients with inadequately controlled COPD and an eosinophilic phenotype.

Ph.D. from a recognized University in subject Pharma, Chemistry, Biochemistry, Biotechnology. Level 11 of Pay Matrix Rs.67,700-2,08,700, 7th CPC Scale.

The applicant needs to attend the Walk-in-interview on the scheduled date & time. Any delay will not be entertained any point of time.

To conduct situational analysis and field visits for enabling informed decision by the states in implementation of the initiative. To assist states and MoHFW in adoption, customization of the IT based Inventory Management system developed by CDAC and NIC e.g. e-Aushidhi, DVDMS etc.