Karnataka

The purpose of the Quality Medical Reviewer role in Medical Affairs is to review and approve medical and promotional materials to ensure they are medically accurate and interpreted correctly based on the review of references, citations and data available.

Post graduate Degree or PhD in Life Sciences, Pharmacology and Biomedical engineering with experience three years in conducting large scale intervention studies.

Market research and analysis of CDMO landscape, Biologics, Biosimilars and Small Molecules business. Refer databases, news, articles etc and generate leads for potential business, newer technologies etc. Reach out to leads and present about One Source Capabilities.

To provide undergraduate engineering or postgraduate science student with an opportunity to engage in advance research and gain hands-on experience in the project

Responsible for analysis and documentation of Bioassay samples of finished products and stability samples.

Bachelor degree in a scientific, health, communications, technology health related field.Demonstrated experience in technical, regulatory scientific writing.

Within this program you will thrive within a fast-paced, dynamic study design. As we are fully embedded with this global pharmaceutical client, you will experience a true one team approach that provides limitless opportunity to develop through training, mentorship, and support from leadership.

Create and review regulatory documentation for Drug, Device and Combination product renewals and other life cycle maintenance-related submissions. Interact with non-regulatory support groups

B.Pharm, M.Pharm, Pharm.D or BDS.; Working knowledge of literature case processing, drug safety regulations and adverse event reporting