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.

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

Supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support to CDMs, according to GCDMP guidelines, local regulatory requirements and Novotech, Client SOPs. 

M.Sc, M.Tech, M.Pharm with prior experience in Quality Assurance with 5-10 years in GMP pharmaceutical organization