Regulatory Affairs Assistant Manager

Company DescriptionAce Cathtech Pvt Ltd, established in April 2024, is a cutting-edge manufacturer of premium medical devices, specializing in Nephrology Products, Cardiac Surgery Equipment, Critical Care, and Anesthesia Products. Located in Faridabad, Haryana, our state-of-the-art facility adheres to the highest manufacturing standards, including a Class 7...

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...

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...

Company DescriptionPacific OneHealth redefines healthcare with India's innovative micro hospital model, providing advanced infrastructure, state-of-the-art diagnostics, and multidisciplinary expertise. Focused on delivering personalized care, Pacific OneHealth ensures that every patient receives customized attention. With a commitment to quality and...

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...

About The JobPosition Title: Assistant Manager (Legal & Corporate Affairs)Reporting to: Head - Legal / Company in-house CounselDepartment: Legal & Corporate AffairsLocation: Aerocity, New DelhiKey Responsibility AreasContract Drafting, Review, and NegotiationDraft, review, and negotiate a wide range of commercial contracts, including:Service AgreementsVendor...

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....

The Regulatory Documents Assistant will establish and maintain the Sponsor electronic or paper Trial Master File (TMF) throughout the life of the trial and will perform record review of essential documents for accuracy and quality according to ICH-GCP. The Regulatory Documents Assistant is also responsible for the set-up of the Investigator's Study File...

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...