Hyderabad

Maintain smooth collaboration and works closely with key stakeholders across the globe to develop reference standards for biotechnology pharmaceutical products including proteins, peptides, heparins, antibiotics, and advanced therapies.

Quality Assurance - in process - Drug Substance Manufacturing, Upstream, Downstream

Prepare clinical regulatory documents for public disclosure, including anonymization of personal data and redaction of commercially confidential information

B.Pharmacy, M.Sc Analytical, M.Pharmacy Analytical ; Selected candidates must commit to a three-year service agreement.

Support a discipline and or provide a service individually or within a team of associates. May provide functional expertise to Line Unit and other QA Units in area of responsibility

post graduate degree, preference given for Ph.D. in Organic Chemistry or Medicinal, Pharmaceutical Chemistry area. National Institute of Pharmaceutical Education and Research

Doctoral degree in Science, Pharma from a recognized University or Equivalent with two years of experience in analysis of high throughput genomic data.

Ph.D. in Environmental Engineering, Biotechnology, Microbiology, Chemical Engg, Climate Change or other allied areas.  Experience with handling chromatography instruments preferred. 

Masters degree in Natural or Agricultural Sciences, MVSc or Bachelors in Engineering or Technology or Medicine from recognized University or equivalent.