Ph.D./ MD / MS / MDS or equivalent degree or having 3 years of research, teaching and design and development experience after MVSc / M.Pharm / ME / M.Tech with at least one research paper in Science Citation Indexed journal.
M.Sc. in Microbiology/ Biotechnology from a recognized University. Candidates having hands on experience in handling microbes, enzymes and fermentation techniques will be preferred.
Strong knowledge of Quality Agreement / Technical Agreement drafting and review. Practical experience in vendor risk assessment, approved vendor list management and periodic vendor requalification.
Work as a partner with the global study leader to monitor study conduct and progress – identify, resolve, and escalate risks that impact delivery of the study against quality, timeline, and budget objectives.
For more than 130 years, we’ve brought hope to humanity through the development of important medicines and vaccines. We foster an inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities.
Manage and review expeditable adverse events, product quality complaints and medical information to the required standard and submit them to the client and the regulatory agencies (if required) within the agreed/stated timelines.