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
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
Candidate should have knowledge of manufacturing operations of granulation, compression, coating and capsule filling, responsible to adherence cGMP guidelines. USFDA, MHRA exposure is must.
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.
IIHMR University, a leading health management research university in India, on July 20 th successfully wrapped up its Annual Convocation, at the pristine campus in Jaipur, Rajasthan. The momentous occasion marked a milestone event in the lives of 334 students who were conferred with their well-deserved degrees.
Provide practical, hands-on experience with AI tools in educational and research activities. Address the challenges and opportunities of integrating AI tools in higher education settings
D.Pharm, B.Pharm, M.Pharm
Age 18 to 32 years as on 1.1.2024. Provided that in case of candidates belonging to Scheduled Tribes and Scheduled Castes of Meghalaya, the upper age limit shall be relaxableby 5 years
Under the District Program Management Unit, the following staff posts have been advertised to be filled on a purely temporary basis for 11 months on contractual basis and to create a waiting list for the same. Validly qualified candidates dt. 22/07/2024 to Online application has to be done on Arogyasathi software link arogyasathi.gujarat.gov.in till 06:00 PM till 27/07/2024.