Executive/ive Regulatory Affairs

Company DescriptionMove Ahead Consultancy (MAC) is a leading firm specializing in providing comprehensive solutions for Regulatory Compliance in industries such as Food, Cosmetics, Medical Devices, Legal Metrology, as well as Imports & Customs Clearance. With over 14 years of expertise and a strong presence in New Delhi, MAC is dedicated to simplifying...

EXECUTIVE -REGULATORY AFFAIRS Export Regulatory Affairs will be responsible for managing and coordinating regulatory submissions, product registrations, and compliance activities for international markets. This role ensures that all documentation and submissions meet the regulatory standards and timelines of target export countries, while supporting business...

Zoot Systems is a New Delhi, India based company. For years, it has been our continuous endeavours to understand Client quality-conscious discerning business needs and to successfully meet those. We specialize in the creation of high-quality I.T./Non-I.T. based HR Solutions, Recruitment, and RPO to companies of all sizes resulting in better, faster, and more...

About WebcardioWebcardio is a leading provider of innovative cardiac monitoring solutions, offering Doctors and patients real-time, remote cardiac diagnostics through advanced wearable ECG technology. Our mission is to improve cardiac care delivery using AI driven insights and seamless technology.Role OverviewThe Medical Affairs Manager will lead and oversee...

Position:DM / MGRFunction:Corporate Affairs (CPA)Experience:~3-7 years (preferably in the auto industry)Location:Maruti Suzuki Head Office, Vasant KunjRole Overview:We are looking for a dynamic, sharp, and self-driven professional to join our growing Corporate Affairs team. The role involves translating complex automotive policy issues into clear, compelling...

Prepare and submit regulatory submissions, including product registrations, variations, renewals, and licenses to various Authorities in different countries. Apply and manage CDSCO licenses (e.g., ISO 13485, MDR 2017/745, US FDA, etc.). Required Candidate profileExcellent written and verbal communication skills with the ability to produce high quality...

Experience:1-2 YearsLocation:Rohini Sector-3, New DelhiCompany:ELT Corporate Private LimitedCompany DescriptionELT Corporate Private Limited is India's leading regulatory and market-access consulting company, assisting manufacturers, importers, and exporters in obtaining statutory certifications such as BIS, Legal Metrology, CDSCO, CE,USFDA,EPR, and AEO....

Job Description: -Relationship-building, liaison, and obtaining licences, permits, and approvals related to the company's business.The ability to coordinate with statutory organisations, such as Mantralaya, State Departments (Energy, Revenue, Home, Industry, State Nodal Agencies, SLDCs), and Local Administration (at the district level), to carry out...

Role & responsibilitiesResponsible for CDSCO, DCGI, state FDA work compliancesCoordination with CDSCO to get clarity on few of our products whether they are under new drug or old drug.Preparation and online submission of BA/BE NOC application to CDSCO.Preparation and online submission of CT-10 for manufacturing the new drug (Indore & Bhiwadi).Preparation and...

**Organization OverviewThe organization is a leading consulting firm with a proven track record of partnering with some of the world's top companies. The firm has built a reputation for credibility, trustworthiness, and delivering solutions.**Roles & ResponsibilitiesRole· Strategic Affairs is a dynamic, proactive professional responsible for supporting the...