Hyderabad

Experience into Complex Injectable and Complex Equipment like HPH, Isolator, Wet Mill, ANFD. Experience in injectable and Ophthalmic dosage form like suspension & Gel forming and simple ophthalmic range.

Redaction of clinical trial documents in accordance with evolving global regulations. Develop training and drive change management for novel processes related to the EU Clinical Trial Regulation and other regulations. Manage and Coordinate redaction of clinical documents in accordance with EMA Policy 0070, Health Canada Public Release of Clinical Information, PRCI, EU Clinical Trial Regulation, and other global regulations. 

Support Analytical project leader for setting analytical development strategy. Support in data interpretation, results compilations and sharing the information with critical observations and proposals to project team.

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.