Provide technical support to the DteGHS, Ministry of Health & Family Welfare by implementing the priorities of the WHO-Global Patient Safety Action Plan 2020-2030 & National Patient Safety Implementation Framework. Facilitate in coordination with the Center of excellence to include Patient Safety activities in their State PIPs under the guidance of MoHFW.
B.Pharmacy Or Approved Diploma in Pharmacy. ECHS invites applications to engage following OIC, Medical, Para-Medical and Non-Medical Staff on contractual basis in ECHS Polyclinics, Imphal & Churachandpur
M. Pharma / B. Pharma; Awareness of regulatory requirement, ANDA filing & new Product filing application, Handle Field Alert Report, Market complaint, Review & presentation of Data, Tracking of data. Planning for sample pullout, Batch charging, storage & reconciliation, destruction & smooth functioning of Stability chamber, Walk-in Chamber
Transcriptorric and functional analysis of myeloid compartment in patients with X-linked agammaglobulinemia. First Class Post Graduate Degree, including the integrated PG degree or PhD. Candidates with hands-on experience in flow cytometry, Data analysis and inteipretation and single-cell genomics / transcriptomics will be preferred
Candidate will be expected to have worked with primary cells and cell lines in immunology or immuno-oncology context. Prior experience working in development and validation of cell and gene therapy products will be preferred. M.Sc / M.Tech in Biotechnology
Analytical method validation of different methodology. Dissolution Method Development and validation. Validation and method development protocol and report preparation.
Stallion Laboratories incorporated in 1988 as an integrated private sector Pharmaceutical Formulation Manufacturer, has acquired an unmatched record of managing niche product in formulations with a WHO GMP approved production facility and GLP qualified stringent quality control.
Formulation development of Injectable including development, execution, filing and approval of Complex Injectables viz. Liposomes, Peptides, long acting emulsions, suspensions, in-situ gels, Lyophilised injectable etc.
Natco Pharma is an Indian multinational pharmaceutical company based in Hyderabad. The company manufactures finished dosage formulations active pharmaceutical ingredients and crop health science products, and also provides contract manufacturing services.
Basic Microbiology, Media preparation, Autoclave, Gram staining, Anti microbial tests etc. GPT, BET, VITEK, Bl ENUMERATION, Bio burden. HPLC Analysis. Handling of UV, Elisa Technique, Stability study.
Patients with metastatic colorectal cancer harboring BRAF V600E mutations benefitted from first-line treatment with the targeted therapies encorafenib and cetuximab plus a mFOLFOX6 chemotherapy regimen, according to results from the Phase III BREAKWATER trial led by researchers at The University of Texas MD Anderson Cancer Center.
Statins, a class of cholesterol-lowering drugs, have no effect on kidney function, a research team led by the University of Iowa has found. The research team, led by clinical professors Michelle Fravel and Michael Ernst, in the College of Pharmacy, examined the association between statin use in older adults and changes in two important indicators of kidney function estimated glomerular filtration rate and urine albumin-to-creatinine ratio.
MBBS, Doctor of Pharmacy, M.Sc. Statistics, M.Sc. in Life Sciences with 2 years of experience in the field of systematic reviews, network meta-analysis is mandatory.
B.Pharmacy form recognized institute OR Approved Diploma in pharmacy from recognized by the pharmacy council of India and registered as pharmacy under the pharmacy Act 1948.
MSc or PhD in Life Science with specialization and or work experience in Molecular Parasitology, Genome Engineering, Cell Biology, Biochemistry and Bioinformatics
The candidate needs to be involved with trial registration, participant screening, recruitment, obtaining informed consents, maintaining longitudinal follow-ups using REDCap forms, ensuring GCP compliance, conducting periodic review meetings with site PIs and trial coordinators, troubleshooting issues, review data and generate reports periodically and draft manuscripts, publication materials, engage with stakeholders for recruitment campaigns and manage funding body requirements.
B.S. 4 years programme, B.Pharm, MBBS, Integrated BS-MS, M.Sc, BE, B.Tech or equivalent degree, with 55% marks and passing of NET, GATE test. Project FISHING OUT MECHANORESPONSIVE HYDROGELS THROUGH CHIRAL ORCHESTRATION IN AMOHIPHILIC PEPTIDES : A POTENTIAL THERAPEUTIC TO CANCER AND MICROBIAL CHALLENGES
Conduct QC testing on raw materials, packaging, stability, in-process, and finished products. Capable of Handling Instrument like HPLC, GC,KF, IR,UV instrument. To review analytical data & handling of QMS i.e. Deviations, 00S, 00T, Laboratory incidences, OOC, CAPA and Effectiveness of CAPA.