Position : Senior Executive - Regulatory Affairs
Location : Andheri (E), Mumbai.
Experience: 6 to 8 years
Work from Office - 6 days (Mon-Sat)
Responsibilities :
Manage dossier submissions globally for medical devices.
Coordinate device approvals with Ministries of Health and handle related queries.
Collaborate with R&D and Plant QA/RA for dossier compilation.
Communicate with distributors/consultants worldwide for securing approvals.
Assist in international registration with the Sales Team for country-specific registrations.
Maintain and update submission records with precision.
Prepare and monitor QMS documentation for audits based on individual country requirements.
Meril is a multinational medical device company with its headquarters in India that was founded in 2006 with the goal of creating innovative, therapeutically useful, and cutting-edge technologies. Our primary goal as a top provider of healthcare solutions is to promote the reduction of pain and enhancement of life. We are dedicated to R&D, innovation in medical technology manufacture, scientific communication, and modern distribution channels in order to make this possible.
The Bilakhia Group founded Meril with the goal of enhancing human life quality with cutting-edge medical innovations. As a producer of medical equipment, we work to increase innovation in the field so that people's lives are improved. We always aim to be the best at answering some of the most difficult topics in medicine.
Currently operating in over 100 countries, Meril, a company owned by Bilakhia Group, has its headquarters located in India and employs over 4,000 people. Germany, Brazil, Russia, South Africa, Bangladesh, India, and Turkey are among the countries where we have 100% subsidiaries. Japan and China are also places where we operate.