Life Sciences

Masters degree or an equivalent in any branch of Life Sciences/Microbiology/Biochemistry/Biotechnology/Molecular Biology or any other related field with two years’ post-master’s degree

Coordinate with Regulatory Affairs, Medical Writing, CMC, Quality, Clinical, Pharmacovigilance, and other stakeholders to ensure submission readiness.

Support maintenance of the Dutch WDA license in collaboration with the external RP service provider. Ensure all documentation required for WDA compliance is complete, current, and accessible.

Homi Bhabha Cancer Hospital & Research Centre, Aganampudi, Visakhapatnam recruitment; Graduate in Science E.g. B.Pharm, Life science, B.Sc., Biotech, Zoology, Botany, etc., with PG Diploma in Clinical Research is preferable.

A degree in Life Sciences, Nursing, Pharmacy, Regulatory Affairs, or Chemistry (or equivalent experience that tells a similar story)

Develop and maintain QMS for Medical Device clients; Develop regulatory strategies, submissions and compliance activities for Medical Devices clients; Control, prepare, track and archive quality and regulatory documentation for MD clients

First-class post-graduate degree (M.Sc./MS) in Life Sciences / Chemistry with a minimum of 3 years of experience, of which at least two years should be in the area of developing Lateral flow devices. NIPER Hyderabad

PhD in Biotechnology/Biochemistry/Zoology/Microbiology/Cellular & Molecular Biology/Life Science from Indian universities/Institutes with NIRF ranking of up to 20 or those who have done Ph.D. from abroad with a strong experience. SRICC-BHU

BE, B.Tech, M.Sc, M.Tech. in Biotechnology / Life sciences / Bioinformatics, M.Pharm / M.V.Sc. or equivalent with First Division. The candidate must be a resident of Uttar Pradesh.