B.Pharm / D.Pharm from a recognized University; District Health Society Dwarka has announced to fill up the following posts on contract basis for the next 11 months with fixed monthly remuneration and to create a waiting list for the same.

M.Pharm, Ph.D. in the concerned subject OR Post-Graduation in Ayurveda, Homoeopathy, OR Degree qualification in the respective AYUSH System, Allopathy; Exploration of physiological action of homeopathic anti-anxiety drugs on anxiety mediating human GABAergic and serotonergic neurons

M.Sc Biotechnology, M.Pharm Biotechnology with first class and preferably GPAT qualified. Experience in cell culture, basic molecular biology techniques. project on Development of a low-cost diagnostics kit based on miRNA detection for hepatocellular carcinoma

Masters Degree in any stream of Life Sciences along with NET, GATE and two years of research experience. Masters Degree in Biotechnology, Life Sciences, Biochemistry, Allied biological Sciences discipline; Transition metal-catalyzed fluorine insertion in small organic molecules; Design and Synthesis of Biased Kappa Opioid receptor Agonists for treating Chronic Pain

M.Sc, M.S. in Chemistry from recognized university or equivalent. Research experience in the organic synthesis will be preferred. Active Pharmaceutical Ingredients for Affordable Health Care

Preparation of Freedom to operate opinion for various jurisdictions including USA, Australia, Brazil, China, and EMB markets

M.Pharm / M.Sc; A thorough knowledge related to development, and analytical troubleshooting for Ophthalmic, Injectables and NDDS formulations. In-depth analytical knowledge of techniques and operations viz HPLC, GC, LCMS, PSD, IVRT, Extractable-Leachable.

As a Scientist, Clinical Trial Safety, you will play a pivotal role in reviewing large amounts of clinical data to ensure patient data is complete and medically accurate. support the team during study start-up activities, review patient-level clinical/safety data on an ongoing basis, schedule and facilitate different types of meetings, and create visualizations from applicable tools.

In this role you are required to solve routine problems, largely through precedent and referral to general guidelines. Your primary interaction is within your own team and your direct supervisor 

Whether or not a person becomes seriously ill with COVID-19 depends, among other things, on genetic factors. With this in mind, researchers from the University Hospital Bonn UKB and the University of Bonn, in cooperation with other research teams from Germany, the Netherlands, Spain and Italy, investigated a particularly large group of affected individuals.

Acute myeloid leukaemia is one of the deadliest cancers. Leukaemic stem cells responsible for the disease are highly resistant to treatment. A team from the University of Geneva UNIGE, University Hospital of Geneva HUG, and Inserm has made a breakthrough by identifying some of the genetic and energetic characteristics of these stem cells, notably a specific iron utilisation process.

B.Pharma or equivalent degree with first class from a recognized University, Pharmacy Institute. Knowledge of Hindi. Post Graduate Degree in the relevant subject.

MPharm in Pharmaceutics, Industrial Pharmacy or related discipline with experience in drug delivery systems, dosage form development, HPLC analysis, cell line studies, animal studies, etc

B.Pharm with minimum 1-year experience OR D.Pharm with minimum 3 years working experience in Dispensary, Pharmacy of the Hospital having minimum 200 beds.

Candidates having Ph. D. degree awarded in Bioinformatics, Biotechnology, Botany, Life Sciences, Plant Molecular Biology or equivalent and fulfilling the guidelines of DST Office Memorandum number SR, S9, Z-08, 2018 dated January 30, 2019 are eligible to apply

A strong understanding of regulatory affairs principles, guidelines, and processes of ROW Market Compare and evaluate offers from suppliers. Familiarity with the applicable regulations and requirements in the specific industry or country Track orders and ensure timely delivery

Should exhibit strong Leadership Qualities and holds sound knowledge of current guidance of various regulatory agencies

Batch Disposition post reviewing the batch manufacturing, packing, and testing records assuring compliance with established SOPs, specifications, and standard formats and ensures that all investigations related to batch are closed prior to the batch disposition.

Experience in reviewing specifications and STPs, ensuring data integrity, proposing QbD Quality by Design process changes, and participating in phase gate reviews