Masters degree in Pharmacy, Veterinary Sciences (Pharmacology and Toxicology). Hand on experience in animals handling, dosing, formulation and sampling
BACHELOR OF PHARMACY, BACHELOR OF SCIENCE (B.Sc Degree ), MASTER OF PHARMACY, MASTER OF SCIENCE. Understanding of safety regulatory report documents in terms of purpose of the different sections, data flow and applicable regulations.
M.Sc., M Pharm. B.Sc. Prepares / supports the preparation of highly complex scientific documents to meet highest quality standards. Initiates, implements and champions process improvement techniques.
This role is responsible for providing support to the global regulatory and pharmacovigilance departments regarding regulatory and pharmacovigilance information of the legacy products and sites.
Vivo Bio Tech Limited is a leading preclinical Contract Research Organization based in Hyderabad, India. Vivo is OECD-GLP accredited, AAALACi certified pre-clinical testing facility.
To design and conduct experiments for preformulation, formulation optimization of Microsphere and long acting complex non oral dosage form based on QbD approach.
Manage regulatory audits, customer inspections, and internal audits; ensure effective handling of OOS/OOT, deviations, CAPA, and change control activities.