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Sanofi has launched GLP-1 drug in India

Soliqua is indicated as treatment in adults with obesity and type 2 diabetes mellitus, to improve glycemic control as an adjunct to diet and exercise, in those who are insufficiently controlled on oral or injectable therapies.
Denmark to restrict Ozempic and other GLP-1 drugs for Diabetes
Denmark rationalised cheaper diabetic medicines and restricted GLP-1 analogues. The so-called GLP-1 analogues, which include is known under the product names Ozempic, Trulicity, Rybelsus and Victoza, is significantly more expensive than other types of diabetes medication (so-called DPP-4 inhibitors, SGLT-2 inhibitors, beta-cell stimulants and metformin)
Caprylhydroxamic acid (KOPSYM)- Dual active for Cosmetics
Caprylhydroxamic acid is a synthetic chelating agent that helps protect cosmetic formulas from destabilizing metal ions. It also works as a preservative, having the ability to prevent mold growth in water-based formulas. This ingredient has great flexibility since it works in all types of cosmetic formulas, including waterless (anhydrous) and its efficacy is not pH-dependent.
Job for Degree in Professional Course at AIIMS, Salary Rs. 45,000 pm
Post of Senior Research Fellow under BIRAC - BIG funded project entitled Minimally Invasive Nano-Enabled Targeted Technology for Sentinel Lymph Node (SLN) Detection in Head-Neck Cancer under Prof. Alok Thakar, BIG Grant Awardee
Vacancy for Research Scientist at Rajiv Gandhi Centre for Biotechnology
Creation of a national network of existing and upcoming high risk pathogen laboratories (BSL-3/4) across departments and keeping their interlinkages. 2 years research experience after completion of PhD, in areas related to microbial cell culture (BSL2+), assay development or molecular biology, prior experience in field sample collection, processing, documentation and record
Job for Research Scientist at Tata Medical Center
Develop and refine study designs to ensure scientific rigor and alignment with research objectives. Analyse data according to study statistical plan tailored to the study's specific needs, ensuring that data collection methods align with intended analysis strategies.
Work as Technical Advisor at Government of India Enterprise KAPL
Post of Technical Assistant who have worked in Pharma industries with knowledge of technical and operational activities. Candidates will co-ordinate plant production activities, distribution activities and also will co-ordinate the procurement of material activates, QA,QC and Bulk Drug Project related activities etc.
Multiple Job openings at Centre for Cellular and Molecular Biology
Molecular breeding in rice / Marker-Assisted Selection in rice, Phenotyping of yield, biotic and abiotic stress traits, rice field management, Plant Molecular Biology/Plant-Microbe Interactions using rice plant as a model system 
Zydus Life Sciences Walk in Drive for B.Pharm, M.Pharm in Production, QA, QC Department
For all the positions, it is essential for candidates to have exposure in Injectable Sterile plant and regulatory requirements of documentation as per cGMP/GLP.
Quality Control, Production Jobs at Dr. Reddys Laboratories
Must have exposure in handling of Process Area maintenance like Manufacturing Vassals, Filling machine, Autoclave , Isolators and Lyophilization
Interview for B.Pharm, MSc, BSc in Packing Department at IPCA Lab
Having relevant experience to operation and maintenance of CAM/ IMA/Blister/ CVC/ Cartonator m/c.
Teva looking for Quality Specialist - B.Pharm Apply

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.

Eurofins Scientific Hiring for Assistant Manager

Eurofins Scientific is a group of international life sciences companies which provide a unique range of analytical testing services to clients across multiple industries. The Group believes it is the global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

Walk in Drive for M.Pharm, B.Pharm, M.Sc in Quality Control at Intas Pharma
Having exposure related Environment Monitoring in formulation, water analysis, various Microbiological test like sterility, BET, MLT etc. Having exposure related to regulatory plant and basic know of GLP GMP .Ready to work in rotational shift.
Work as Regulatory Professional at Novo Nordisk - Ph.D, M.Pharm, MSc Apply
You will be a member of a newly established virtual team - EU Submission Hub with colleagues in Denmark, Portugal, Poland and Bangalore focusing on clinical trial submissions in EU. EU Submission Hub is part of Submission Management department, who is responsible for electronic submissions to Health Authorities including New Drug Applications and Life Cycle submissions.
ICON plc looking for Medical Data Reviewer

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success.

ONO Enters into a Definitive Agreement to Acquire Deciphera Pharmaceuticals

ONO Pharmaceutical, Co., Ltd and Deciphera Pharmaceuticals, Inc. announced that on April 29, 2024 (Japan time), ONO and Deciphera entered into a definitive merger agreement under which ONO will acquire all outstanding shares of Deciphera common stock for USD 25.60 per share in cash through a tender offer followed by a merger of a wholly owned subsidiary of ONO with and into Deciphera with Deciphera surviving as a wholly owned subsidiary of ONO.

FDA approves first drug for WHIM syndrome
WHIM syndrome is a rare genetic disease that causes the body’s immune system to not function properly. WHIM syndrome reduces the number of mature neutrophils and lymphocytes (types of white blood cells important in fighting infection) circulating within the body. It is estimated to occur in about 1 in 5 million live births. Approximately 60 cases have been reported in the medical literature.
Lower Dose of Mpox Vaccine Is Safe and Generates Six-Week Antibody Response Equivalent to Standard Regimen
A dose-sparing intradermal mpox vaccination regimen was safe and generated an antibody response equivalent to that induced by the standard regimen at six weeks (two weeks after the second dose), according to findings presented today at the European Society of Clinical Microbiology and Infectious Diseases Global Congress in Barcelona. The results suggest that antibody responses contributed to the effectiveness of dose-sparing mpox vaccine regimens used during the 2022 U.S. outbreak.
Sandoz reaches agreement with Amgen resolving all patent litigation related to its US denosumab biosimilars
Sandoz received FDA approval for the first and only denosumab biosimilars, Jubbonti and Wyost, on March 5, 2024. Jubbonti and Wyost are interchangeable with and approved by FDA for all indications of reference medicines Prolia and Xgeva. They have the same dosage form, route of administration, dosing regimen and presentation as the respective reference medicines.
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