Mumbai

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.

Your function in ensuring data accuracy is critical. You’ll validate ingredient information and toxicological data to maintain consistency across products and platforms. You will connect these elements by adapting to the evolving landscape of consumer safety and seeking innovative ways to manage and communicate ingredient data.

Online Applications are invited for various posts as under NATIONAL CANCER GRID - NCG. Candidates who would be called for Interview are required to carry original documents in support of the details furnished in the online application form regarding date of birth, qualifications, experience, etc., failing which such applicants will not be allowed to appear for Interview. 

M.Sc, M.Tech Zoology ,Medical or Human Genetics, Biochemistry, Molecular Biology, Botany, Microbiology, Biotechnology, Life Sciences, Applied Biology, Cytogenetics. Candidates should have minimum six months experience in Cytogenetics

Plan, execute & ensure timely submission of various applications when assigned including but not limited to only these: test license application, HAQ response submission, CT updates and notification submission e.g. IB amendment, site closure, site addition, EC approval submission etc.

Opportunity in Skin Care Formulation research at Unilever. The role will support all R&D interventions for product development and regulatory compliance within the UI Skin care category.