To co-ordinate with Cross Functional Team for getting various documents required for filing the product in India. Responsible for reviewing CMC documents to be submitted in dossier as per regulatory guidelines.
SunGlow was incorporated in January 2010 and was founded by a group of experienced industry professionals. Our Corporate office is located in Chennai, India.
Bachelors degree in Bioinformatics, Computational Biology, Computer Science, Life Sciences, or a related discipline. Master's degree preferred. Career in Regeneron
To prepare and review documents like Risk Assessment protocols for product change over, Cleaning/Process Validation protocols, Master Formula Records, Batch Manufacturing Records. Review technology transfer documents for Mammalian and Microbial products with coordination with R&D, QC and RA.
Doctorate degree (Ph.D.) in a relevant discipline in the areas of Pharmaceutical Sciences/ Biological Sciences/ Environmental Sciences/ Agricultural Sciences/ Biotechnology or any equivalent discipline, from a recognised University or Institute. National Innovation Foundation
PhD / MD / MS / MDS or equivalent degree OR M.Sc / MVSc / M.Pharma / ME / M.Tech. At least one research paper in a Science Citation Index (SCI) journal. AIIMS
Expertise in Pharmacoinformatics / computational chemistry / Cheminformatics / Bioinformatics, with strong knowledge of the development of various software and web servers in drug discovery and development. NIPER, Kolkata