Hyderabad

Manage R&D development related research for specific Drug Delivery Systems to ensure on-time, within budget quality delivery along with a continuous focus on improvements. The candidate will be responsible for conducting hypothesis testing, designing and developing novel formulations using various materials for diverse applications, including development of Liposomal formulations, Nano- and submicron particulate formulations, Polymeric-Based Formulations, etc.

Masters degree in Chemistry or Biochemistry or Pharmacy or Pharmaceutical Chemistry or Pharmacology or Bacteriology or Medicine or Microbiology or Biotechnology of a recognised university or institute

Filling up of one post of Senior Scientific Assistant Group B Gazetted, Non-Ministerial, in the Pay Level 7 Rs. 44900 - 142400 of pay matrix of 7th CPC in Central Drugs Testing Laboratory CDTL, Hyderabad, Central Drugs Standard Control Organisation, Directorate General of Health Services, Ministry of Health and Family Welfare on Deputation.

Masters, Integrated Masters Degree in Pharmaceutical Sciences or Natural or Agricultural OR bachelors degree in Engineering or Technology or Medicine from a recognized University or equivalent.

To undertake proposed research involving data analysis, computational modeling and programming for the clinical data on diabetes. Experience in data analysis, computer programming and mathematical modeling is desirable.

Exploring how Theileria parasites repress host gene expression PARA- REPRESS. Post Graduate Degree in Natural Sciences with experience in research and development in industrial and academic institutions or Science and technology organizations. Candidate with experience in epigenomics, cancer biology, molecular biology, cell culture, and bioinformatics will be given preference. 

Design, plan and perform scientific experiments for projects at different clinical phases of drug substance and drug product with minimal guidance. Well versed with regulatory guidelines, scientific literature, technology transfer and interpretation of the results to draw conclusions in reports.

Basic knowledge of clinical development, GCP & ICH guidelines, regulations by major regulatory bodies such as FDA, Food and Drug Administration and EMA, European Medicines Agency, and SOPs/ QDs. Review study team-developed documents as per SOP, such as study id card, protocol, amendments, WSI, eCRF Case Report Form and completion guidelines, Centralized Monitoring Plan, committee charters and or other operational documents as requested to provide operational input.

B.Sc./ B. Pharmacy /M.Sc. M. Pharmacy; Preparation and review of Standard operating procedures Retrieval of BPCRs in case of batch cancellation, planning changes. Handling and Execution and investigation of QMS documents in change controls, deviations, and CAPA.