To prepare and review documents like Risk Assessment protocols for product change over, Cleaning/Process Validation protocols, Master Formula Records, Batch Manufacturing Records. Review technology transfer documents for Mammalian and Microbial products with coordination with R&D, QC and RA.
Zydus Lifesciences has announced positive topline results from its global EVIDENCES-X™ Phase II(b) clinical trial evaluating Saroglitazar Magnesium in patients with Metabolic dysfunction-Associated Steatohepatitis (MASH) and fibrosis. The company said the study successfully achieved its primary endpoint, marking an important milestone in its ongoing MASH development programme.
Department of Pharmaceuticals, Ministry of Chemicals and Fertilizers, has announced the second call for applications under the Promotion of Research and Innovation in Pharma & MedTech (PRIP) Scheme, creating fresh funding opportunities for startups, MSMEs and pharmaceutical and MedTech companies working on high-impact innovations.
The Trump administration has announced agreements with nine additional pharmaceutical manufacturers aimed at reducing prescription drug prices in the United States under its Most-Favored-Nation (MFN) pricing initiative.
The latest agreements bring the total number of pharmaceutical manufacturers participating in the administration's MFN arrangements to 26 companies, covering approximately 89% of the branded drug market, according to a White House fact sheet released on August 31.
Doctorate degree (Ph.D.) in a relevant discipline in the areas of Pharmaceutical Sciences/ Biological Sciences/ Environmental Sciences/ Agricultural Sciences/ Biotechnology or any equivalent discipline, from a recognised University or Institute. National Innovation Foundation
PhD / MD / MS / MDS or equivalent degree OR M.Sc / MVSc / M.Pharma / ME / M.Tech. At least one research paper in a Science Citation Index (SCI) journal. AIIMS
The study evaluates the effect of flu and pneumococcal vaccinations in people 60 years and above in the reduction of all cause mortality. This is a randomised controlled trial.
Expertise in Pharmacoinformatics / computational chemistry / Cheminformatics / Bioinformatics, with strong knowledge of the development of various software and web servers in drug discovery and development. NIPER, Kolkata
Masters degree from a recognised University/Institute: M.Sc. Chemistry (Organic/Physical/ Materials/ Medicinal/Pharmaceutical)/ Biotechnology/ Nanotechnology/ Microbiology /Food Technology or related field or M.Pharm / M.S. Pharm (Biotechnology/Medicinal/Pharmaceutical/Process Chemistry). BRIC-NABI
Development and implementation of a Technology-driven AMSP (Anti-Microbial Stewardship Program) Steered by Clinicians to Improve Antimicrobial Prescribing, using mixed-method approach.
Bachelors and Masters Degree in Sciences (Biotechnology, Microbiology, Molecular Biology, Genetic Engineering) / Bachelors Degree in Engineering or Technology (Biotechnology) from a recognized University or equivalent. IIT (BHU)
Masters Degree in Biochemistry, Immunology, Biotechnology, Life science or related fields. NET-JRF or equivalent National-Level fellowship examination qualification is desirable. NII
Ph.D. in Biotechnology / Biotechnology Engineering, Biochemical Engineering, Chemical Engineering, Microbiology, Food Technology, Life Sciences, Environmental Engineering, or any other relevant discipline from a recognized University/Institute. NABI
Masters degree in any branch of : Biotechnology, Molecular Biology, Biochemistry. Minimum 2 years experience in : Cellular reprogramming, Phenotypic characterization, Molecular analysis. SCTIMST
Design and evaluate oncology clinical trial frameworks — including study protocols, patient enrollment strategies, and regulatory compliance considerations
Assist in day-to-day production activities as per SOPs. Conduct basic chemical handling, mixing, and batch processing.
Monitor production processes and record process parameters.