September 2024

Post graduate degree in Life Science. OR Graduate, Post Graduate Degree In professional course e.g., M.Sc. Pharmacology, M.Pharm, MBBS,BDS,BHMS - selected through a process described through any one of the following Scholars who are selected through National Eligibility Test- CSIR-USG, NET including lectureship Assistant Professorship and GATE, GPAT.

The candidate should be M.Pharm Pharmaceutics, Pharmacology In addition to the qualification, the candidate should have the following skills Formulation & Development of Oral tablet dosage forms. Quality Control of Oral tablet dosage forms.

Diploma in integrated Pharmacy course conducted by the Directorate of Indian Medicine and Homeopathy, Chennai

Researchers isolated SARS-CoV-2 strains, which are drug resistant with mutations to the nsp12 protein that is the target of remdesivir and another variant with mutations to the nsp5 protein, the target of Paxlovid. These mutations help the virus persist in people with compromised immunity despite common antiviral treatments.

Researchers from the Mechanobiology Institute at NUS and the NUS Bia-Echo Asia Centre for Reproductive Longevity and Equality , based at the NUS Yong Loo Lin School of Medicine, have developed an innovative technique to significantly enhance the reproductive potential of aged oocytes, or immature egg cells, potentially paving the way for better outcomes of assisted reproductive technologies, such as in-vitro fertilisation , for older females.

Designing and executing Translational research projects and protocols for different Discovery to Innovation Accelerator projects. Perform experiments, collect and analyse data. Maintain accurate record of all the experiments and provide ready access to all data to the reporting authority.

All granulation equipment, compression machine and Auto Coater. Scada PLC Operated Machine RMG, FBP, bag dumping station, preferably have worked with IGL, should have handled all documents in granulation and compression.

Executed end-to-end project management for new product development from project initiation through to filing of the dossier, liaising with cross functional teams to respond to deficiencies and receipt of approval from the regulatory agency.

Supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support to CDMs, according to GCDMP guidelines, local regulatory requirements and Novotech, Client SOPs.