October 2024

Post graduate in M.Sc. Ag, M.Sc., MPharm., M.V.Sc., Bachelor of Engg, Technology B.E, B.Tech, or equivalent degree

Masters degree in Biophysics, Neuroscience, Biomedical Sciences or any other branch of Life Sciences or M.Pharm Pharmacology Scholars who are selected through National eligibility tests-CSIR- UGC NET including lectureship Assistant Professorship or GATE, GPAT.

M.Sc in Chemistry with specialization in organic chemistry, M.Pharm, M.S Pharm in pharmaceutical chemistry with or without NET, NET LS, GATE, Equivalent

Candidates holding Postgraduate, Masters degree M.Sc. ,M.Tech., M. Pharm etc Two Years Course in the area related to life sciences including botany, chemistry, biochemistry, biotechnology, agriculture sciences, microbiology, plant sciences, pharmaceutical chemistry, food technology, or an equivalent degree

Having exposure related Environment Monitoring in formulation, water analysis, various Microbiological test like sterility, BET, MLT etc. Having exposure related to regulatory plant and basic know of GLP GMP .Ready to work in rotational shift.

To supervise and monitor day to day activities of processing and holding of drug product as per define and approved procedures for stability batches and commercial batches.

Contribute to preparation including authoring where relevant and delivery of simple, and with experience, increasingly more complex regulatory maintenance submissions from either a global and, or regional perspective.

The incumbent will be responsible for leading the overall Quality function for the organization. The Head –Quality will guide and lead members of the Quality Assurance and Quality Control teams to deliver as per the corporate goals, projects, plans and timelines.

Regulatory Affairs professionals with 5 to 8 years of experience in regulatory strategy, dossier review, and submission for the US, EU, and Brazil markets.