Hands on Experience in IPQA Manufacturing process and Engineering IPQA, AQA Micro, Documentation, Validations, Stability Management and Document review.
To file amendments and deficiency response within timelines with go getter approach. The job requires review of documents related to DMF submission against predefined checklists and submission to various agencies globally.
Ensure submission and approval of high-quality regulatory applications within planned timelines and Facilitate interactions with regulatory bodies on a regular basis for approvals.
Extramural project Technical Resource Centre under the Centre for Evidence for Guidelines. Postgraduate degree in Public Health, Statistics, Epidemiology, Health Sciences, Environmental Sciences, Life Sciences, Population Sciences, M.Pharm Pharmacy Practice with 3 years of post PG experience in research/projects with at least one research paper in SCI journal.
Postgraduate degree in Public Health, Statistics, Epidemiology, Health Sciences, Environmental Sciences, Life Sciences, Population Sciences, Demography, Health Economics, HTA, M. Pharm Pharmacy Practice with 3 years of post PG experience in research, projects with at least one research paper in SCI journal.
Development and validation of Al-powered voice assistant device for cardiac patients. Post Graduate degree in basic science including the integrated PG Degrees. Should have experience in Clinical Drug trial.
In HPLC, GC, UV, IR, KF & Polarimeter etc. Zuventus Healthcare Ltd. is a dynamic and forward-thinking company that has achieved notable recognition in the healthcare industry and for medical contribution. In OSD manufacturing, packing & QMS
B.Pharm, BSc, MSc; Lincoln Pharmaceuticals Ltd., Ahmedabad based 40 years old, public limited having presence in 75 countries, 1700 registered products, own Manufacturing and R&D center and among indias top 70 pharma company.