Karnataka

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

M. Pharm with 10 years of experience in handling ADME assays and HPLC and LCMS, MS Or Fresh Ph.D. in similar disciplines

Ph.D. in relevant discipline and M.Pharm Pharmaceutical Quality Assurance, experience and good track record of publications, patents. The candidates who have submitted PhD thesis may also apply.