Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidances and defined regulatory strategies.
Masters, Integrated Masters in Natural or Agricultural or Pharmaceutical Sciences OR Bachelors Degree in Engineering or Technology or Medicine from a recognized University
IRG subsumes the Empowerment and Equity Opportunities for Excellence in Science (EMEQ) scheme of erstwhile SERB. IRG will provide enhanced support with flexible norms.
Post Graduate, Masters Degree, M.Tech in Life Sciences Biotechnology, Biochemistry, Microbiology, Etc. NIAB is an autonomous and premier institute of the Department of Biotechnology
Post Graduate Degree in any field of Pharmaceutical Sciences. GPAT or equivalent qualification. At least one year of experience in ophthalmic formulation development, Microneedle-based drug delivery systems
Proficient in routine laboratory techniques like sterile handling, instrument calibration, validation, and documentation. Must demonstrate good written and communication skills.
Maintain effective relationship with the end stakeholders medical scientific community within the allocated Global Business Unit and product – with an end objective to develop education and communication content as per requirement