Executive Or Sr. Executive

2 weeks ago

Vapi, Gujarat, India Meril Life Sciences Full time

About us MERIL DELIVERING WORLD-CLASS HEALTHCARE SOLUTIONS Founded in 2006 Meril is an India-based global medical device company that is dedicated to the innovation design and development of novel clinically relevant and state-of-the-art devices Our fundamental aim is to champion the alleviation of human suffering and improve quality of life To enable this we are committed to R D innovation in manufacturing medical technology scientific communication and contemporary distribution avenues Meril was born with the aim of improving the quality of human life through innovative and advanced healthcare solutions As a medical device manufacturer we exist to improve the inventiveness in healthcare so that people s lives are enriched We continually seek excellence in providing answers to some of medicine s toughest questions Meril manufactures medical solutions in the form of vascular intervention devices orthopaedic supplements in-vitro diagnostics endo-surgery and ENT products It is our core commitment to ensure the delivery of advance healthcare solutions Our inclination towards research and development is reflected in our diverse offerings We ensure that we adhere to the best quality of standards in manufacturing scientific communication and distribution to deliver path-breaking healthcare products to the world We collaborate with physicians and global innovators to identify unmet clinical needs and develop revolutionary therapies We encourage research and academic collaborations and remain available to interact on exciting opportunities Headquartered in India with a manpower of more than 4000 Meril currently conducts business in more than 100 countries We have 100 subsidiaries in India USA Germany Brazil Russia South Africa Bangladesh and Turkey We have set up operations in China and Japan too The JD for the Regulatory Affairs Sr Executive or Executive for International Regulatory Affairs dept will be follows- 1 Dossier collation and submission across the globe for the medical devices for all of the above segments 2 Query handling and liase with various Ministries of Health for the approvals of the devices 3 Coordination with R D Plant Quality Assurance Regulatory Affairs department for the collation of the dossiers 4 Communication with distributors consultants across the globe to get approvals for the devices 5 Coordination with the International Sales Team for the registrations in their respective countries 6 Update and maintain the documentation for the submissions at our end and maintain all records 7 Maintaining and monitoring the QMS documentation and Preparing for Audits as per individual countries requirement Work Experience 1-3 years Industry Medical Device City Vapi State Province Gujarat Country India Zip Postal Code 396191

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