Roles and Responsibilities : Candidate is Responsible for Preparations of Dossiers based on MOH Regulatory Guidelines from Varrious Countries. Organising COPP/FSC /Artwork preparations based on Country Specific Regulations.Communication with Varrious Countries Regulatory for status and Scheduling Registrations of products submitted for Registrations.Preparations of Products Specifications, Loan License Applications, product permissions etc.
Desired Candidate Profile : Candidates should be BSC/MSC/BPHARMA/MPHARMA from Reputed University with Experience of 5 to 10 years in Regulatory (DRA) Section with Similar work Experience , With Good Communication and Coordinations Skills with Internal as well External Agencies.
Candidates should have Good Knowledge of Regulatory work like Dossiers preparations , Regulatory Guideline , Thorough Understanding about products stabilityies of varrious Zone/ Bioequivalence and Clinical Study / Product permission , Literature Search etc.
Kowledge of prepration of Presentations Products charateristics and Properties etc.
Perks and Benefits : Company Has positive Rewarding systems based on Experience ,knowledge, skills. Further Company is having Its Leave Policy IN Place with Good Recruitment History.