Ra Specialist

Designation RA SpecialistLocation - BKCExperience 4 0 Year s To 10 0 Year s Work Time - 9 AM to 5 PMWork Days - Monday to Friday Saturday and Sunday off Salary Best in Industry Other benefits- PF Mediclaim bonus 24 days paid leaves and Bus Facility It will be on role of Talisman HR Solutions Pvt Ltd payroll and on 1 year contractJOB SUMMARY Responsible for all registration activities including submissions into SUGUM Registration System for Medical Devices and Diagnostics for India Market only Provide support to India business managers for regulatory related issues in India Provide strategy to management for rapid product approval and timely market entry into India CORE JOB RESPONSIBILITIES Compile and review regulatory submissions for timely registration of new products renewal of entire range of on-market products for India Ensure product regulatory launch plan is strictly met Provide inputs on possible factors which may impact the regulatory launch plan timeline of new product line for ADD Provide timely inputs when there is a need to modify product launch timeline with adequate time to implement same without any financial resource constraints Identify upcoming evolving regulatory requirements for new IVD product launch Serve as ADD RA representative in industry regulatory meetings To maintain good contact and ensure timely follow-up with Indian regulatory agencies Determine the scope of information documentation necessary to file new registration applications and post-approval changes according to existing checklists to regulatory agencies Review product labelling material for compliance with applicable regulations and standards Ensure regulatory project deadlines and performance standards are established and met Ensure timely submission of products at NIB for performance evaluation of products for the purpose of registration Draft processes for new regulatory requirements towards effective implementation Coordination for Local testing for the purpose of generation of performance evaluation reports from Central Medical Testing Laboratory Ensure receipt of IVD kits for submission to National Institute of Biologicals Noida follow up of reports and communication of related issues to Abbott and coordinate with NIB for newer plans of testing and improving future business relations with NIB etc Ensure receipt of Invoices against payment done Minimum EducationBachelor in Pharmacy B Pharma Graduate Post Graduate Biochemistry Biotechnology Microbiology Immunology Medical technology pharmacy Pharmacology is preferred Masters in above field will be preferred