Supporting RA Team for the Indian Sub Continent to ensure on time registrations, monitoring and assessment of changes in regulations, review of product changes and regulatory assessment, ensure compliance to applicable regulations.
Responsible for planning, supporting RA Submissions, approvals, renewals and compliance to applicable act and rules under following ministries-
1. Ministry of Health (CDSCO) - D&C Act and Medical Device Rules,
b PC&PNDT Act and Rules
2. Atomic Energy Regulatory Board;
3. Ministry of Communication and IT (DOT)- Wireless Approvals
4. Bureau of Indian Standards- ISI Marking and Accessories required to comply with METY registration order (Registration marking registration Scheme)
5. Ministry of Environment and Forest- Preowned Medical Equipment
7.Ministry of Electronics And IT- (MIETY)
12. Ministry of Chemicals and Fertilizers- NPPA Compliance as per Drugs Price Control Order (Notified Medical Devices are regulated as Non-Scheduled formulation)
13. NMRA (Sri Lanka) -National Medicine Regulatory Authority
14. DGDA (Bangladesh) - Directorate General Drug Administration
Support RA manager for Operations / supply chain in addressing regulatory queries from customs
Support to Govt Sales team in addressing regulatory queries/ clarifications
Support to customers query with regards to AERB compliance, customs with regards to CDSCO, AERB, BIS act and rule compliance
Coordinate with regulators, test lab and govt for facilitation of clearance from BIS for electronic accessories.
To succeed in this role, you should have the following skills and experience
A university degree in Science or Engineering with minimum of 6 - 10 years experience in Regulatory Affairs with -
Working knowledge of relevant India and international medical device regulations ( CDSCO, BIS, AERB, MIETY, MOEF, Min of Consumer Affairs, Ministry of Chemicals and Fertilizers, and Ministry of Health (PC&PNDT)
Knowledge of Health Care standards applicable to Diagnostic X ray, Electric safety, risk management, software related standard (Global & Local Standard)
Problem solving skills for regulatory, quality and product safety issues.
Demonstrated ability to balance business needs and regulatory perspective.
Able to develop strong relationships with their country Competent regulatory body(ies) to support open communication with regards to vigilance and recalls, as appropriate
Knowledge of ISO 13485 & 9001, 60601 and other standards