GLP, Raw Material -Packaging Material, In Process-Finished Product, Method Verification Protocol preparation & Document Section Knowledge required; Water sampling/testing, EM Observation, Culture Handling, Media Management, Having Digital exposure for LIMS/ MODA Software B.Sc/ M.Sc/ B.Pharm; Lead QC operations as Shift In-Charge. Review analytical data, Ensure compliance with LIMS, GLP, ALCOA ICH/FDA

Towards Discovery and Development of Novel Drugs and Pharmaceuticals. Experience in Natural Product Isolation and Characterization, Evident from Publication. Organic Synthesis, Natural Product Isolation, HPLC analysis.

ICMR funded extramural project titled Polymeric nanomedicine mediated inhalation therapy to treat chronic obstructive pulmonary disease (COPD) related inflammation; M.Sc. Biotechnology / Bioengineering / Biomedical Science; M.Tech. Biotechnology / Bioengineering / Biomedical Engineering; M.Pharm. Pharmaceutics / Pharmaceutical Technology

Required Trial Coordinator under Resonance Research Capacity Building; Post Graduation in Science M.Pharm, Life Sciences, Biotech, Zoology, Botany, etc. with PG Diploma in Clinical Research is mandatory. The Tata Memorial Centre, TMC is a Comprehensive Cancer Centre with a mission to achieve the highest standards in patient care, cancer prevention, cancer research and professional development for oncology and allied disciplines.

Synthesis and Evaluation of Nitrogen Tethered Derivatives in Cell-Based and Animal Models of Acute Lung Injury. The candidates should possess an M.Pharm/ M.S. Pharm./ M.Sc. in Chemical Science/ Medicinal Chemistry /Pharmaceutical Chemistry/ Pharmaceutical Sciences/ Chemistry/ Biochemistry or a PG degree in other relevant branch of Chemical Sciences.

diploma in pharmacy with experience in a hospital of repute. Must have registration with the state or Central Pharmacy Council; Institute of Liver and Biliary Sciences, ILBS is an autonomous super-specialty Institute of excellence under GNCT of Delhi and a Deemed-to-be-University by the UGC.

ICMR Extramural project titled Study on the Pharmacological Inhibition of Human Sperm GSK3a and Calcineurin on Fertilization Parameters to Develop Male Contraceptives at the Manipal Centre for Biotherapeutics Research. M.Sc. Biotechnology / Biochemistry / Microbiology / Molecular Biology/Genome Engineering/ Medical Biotechnology/ Biomedical Science / Life Science,  M.Tech. Biotechnology / Biomedical Engineering,  M.Pharm

Delineating and characterizing the m6A RNA methylation marks in primary and relapsed B-cell Acute Lymphoblastic Leukemia; MSc Life Sciences research experience or PhD in life sciences; Hands on research experience in molecular biology experiments PCR, Real Time PCR, Cloning, bioinformatics analysis of transcriptomes, exomes, custom analysis is desirable.

A multi-omics approach to delineate the role of neutrophil and plasma indicators in the progression of sepsis and predisposition to early mortality in Severe Alcoholic Hepatitis, SAH Patients. First class post graduate degree including integrated PG degrees

A post graduate degree in any discipline, preferably related to Medical or Allied and Healthcare education or healthcare policy or health administration or public health from any University with outstanding ability and proven administrative capacity and integrity.

A Randomized, Double-blind, Parallel Group, Multi-center, Phase III Study to Assess the Efficacy of Budesonide, Glycopyrronium, and Formoterol Fumarate Metered Dose Inhaler Relative to Glycopyrronium and Formoterol Fumarate MDI on Cardiopulmonary Outcomes in Chronic Obstructive Pulmonary Disease

Looking for clinical Database Developer experience in eCRF build and edit checks build in Veeva studio; Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process. Providing support for the mapping and transformation of clinical data to CDISC SDTM standards. Work independently and accountable for study Data Management deliverables; Coordinate with Biostatistician, Clinical, Medical and local study team as applicable

Responsible for designing overall marketing and communication strategy of brands; Good at Sales & Market data analysis; Must possess knowledge of product strategy, product launch. Torrent Pharmaceuticals announces hiring for a Product Management Team; B.Sc. /B.Pharma plus MBA

B.sc/ B.Pharm/ M.Pharm/ M.Sc; Instrument Analysis HPLC, GC, LCMs, GCMs / Microbiology Testing. Production, QC, Warehouse OSD Formulations

M.Pharmacy / M.Sc. / BPharm; Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non-conforming samples, CAPAs, data evaluation and reporting. Write cGMP Quality documents including Standard Operating Procedures, laboratory equipment procedures and investigational protocols.

Galderma today announced that the United Kingdom (UK) Medicines and Healthcare products Regulatory Agency and Swissmedic have granted the marketing authorization of nemolizumab for the treatment of both atopic dermatitis and prurigo nodularis in the UK and Switzerland, respectively. Specifically, the approvals are for nemolizumabs subcutaneous use for the treatment of moderate-to-severe atopic dermatitis in combination with topical corticosteroids and/or calcineurin inhibitors

Thousands of single changes in the nucleotides that make up the human genome have been associated with an increased risk of developing cancer. But until now, its not been clear which are directly responsible for the uncontrolled cellular growth that is the hallmark of the disease and which are simply coincidences or minor players.

MED-EL USA announced that the U.S. Food and Drug Administration approved the new SONNET 3 audio processor for MED-EL cochlear implants. SONNET 3 is the companys lightest and smallest behind-the-ear audio processor and features integrated wireless direct streaming capabilities.

A Diploma in Pharmacy or Bachelor of Pharmacy or Pharm.D; Must have registered with Tamil Nadu Pharmacy Council and must keep the registration alive by renewing it regularly every year. For the Pharmacist who have worked in Government Medical Institutions during COVID 19 pandemic for a period of minimum of six months to one year continuously without break in service