Ph.D. degree in respective discipline, with a consistently good academic record throughout. Candidates who have submitted the thesis and awaiting award of degree may also apply.
To lead and manage all regulatory affairs activities at the manufacturing site located at Mumbai and LL locations, ensuring timely regulatory submissions, compliance with regulations, and providing strategic support to institutional and international business operations.
Job Description typically involves ensuring injectable pharmaceutical products meet safety and quality standards through testing, documentation, and compliance with regulatory guidelines like GMP.
This role provides regulatory leadership across the organization, ensuring compliance with FDA regulations and guidances, while driving continuous improvement in lifecycle management processes.
May enter data or assist in the creation of cases into the safety database in accordance with Sponsor, customer specific guidelines and Company standards if required.
For a few dozen people in the world, the downside of living with a rare immune condition comes with a surprising superpower—the ability to fight off all viruses. Columbia immunologist Dusan Bogunovic discovered the individuals’ antiviral powers about 15 years ago, soon after he identified the genetic mutation that causes the condition.
A new study has shed light on how a type of drug works to reduce liver damage in alcohol-related liver disease, by reshaping the architecture of the tissue. The findings could pave the way for the development of new treatments for liver disease and improve outcomes for patients.
B.Pharm with minimum 01 year of experience OR D. Pharm with minimum 03 years’ experience. Experience in Dispensary / Pharmacy of the Hospital having minimum 200 beds.
PhD, MD, MS, MDS or equivalent degree or MVSc M.Pharm, ME, M. Tech, M.Sc with at least 3 year of research experience and one research paper in Science Citation Indexed Journal.
Doctorate (PhD) in Chemistry / Materials Science / Chemical Engineering or equivalent degree or having 3 years of research, teaching and design and development experience after MVSc / MPharm / ME / MTech.
Postgraduate degree in science (M.Pharma, Life Science, Biotech, Zoology, Botany etc.) with PG Diploma in Clinical Research with two years Experience is mandatory.
Masters degree in Microbiology / Biotechnology. Basic knowledge of PGPRs, microbial community-NGS, skills, ethics to execute, deal with the experimentations