Mumbai

Ph.D in Pharmaceutics / Pharmacology / Nanotechnology / Biotechnology with experience in nano formulations. Post doctoral Fellow; Experience in development and characterization of nano drug delivery systems, handling cell line studies and small animals desirable.

experience in Pharmaceutical, CRO or Biotech industry; clinical drug development within the pharmaceutical industry or related industry.

RA publishing will participate in the publishing of different regulatory activities. The focus will be to ensure 100% quality and timeline of the submission. This role will be the primary interface with the Regulatory Affairs Associate

The candidates should mandatory have extensive experience through their PhD or other trainings in working with transplantable or inducible mouse models of cancer, and be well-versed in multi-colour flow cytometry. The candidates should be well-versed with regular laboratory techniques, which include but are not limited to western blotting, Immunohistochemistry, qPCR, etc

B.Pharm degree from a recognized university. Registration Certificate of Pharmacy Council Valid registration certificate as per Pharmacy Act, 1948 is required.

Sr. Quality Specialist, Clinical Quality responsible for managing clinical quality function, ensuring compliance with local clinical trial regulatory requirements and Takeda Quality Management Systems. Works in collaboration with local clinical operation team ensuring adherence to Good Clinical Practice Guidance.

Developing Precision Immunotheraphy for Value –Based Treatment of Lung Cancer in India. Graduate, Post Graduate in Life Science with a Diploma in clinical Research. MSC in Clinical Research. 1 - 2 years of experience in Project Management is Mandatory. Experience in drafting of study progress and fund utilization reports is Desirable.

Post Graduation Degree in Life Science, Biotechnology, Biostatistics. Prior experience in clinical or translational research.

Perform real-time monitoring of production processes to ensure adherence to quality standards. Conduct routine inspections and in-process checks to verify compliance with specifications and protocols.