Regulatory Affairs Associate

Hiring Now: Executive Regulatory Affairs Are you ready to take your career to the next level in regulatory affairs?Join our team and play a pivotal role in ensuring compliance and excellence in the medical device secto Key Responsibilities:-Prepare and review CTD, ACTD, and TCF dossiers with precision.-Review critical technical documents such as:-Process...

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...

 Experience in medical device regulatory document preparation including Clinical Evaluation Report, Post-Market Surveillance Report, Post-Market Clinical Follow-up Plan/Report, Periodic Safety Update Report (PSUR) for Medical devices, Summary of Safety and Clinical Performance (SSCP) Report etc. Skilled in Materiovigilance activities and reporting in...

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...

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...

JOB PURPOSE The role of Lead Policy & Regulatory for GMR Renewables will Keep a close track of Open access (Third party and Captive) Policy and Regulatory developments, analyze notification/judgements across states in C&I space and ensure our interest is protected / represented via. Timely inputs to relevant internal / external stakeholders, via various Wind...

**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...

Ready to shape the future of work?At Genpact, we don't just adapt to change—we drive it. AI and digital innovation are redefining industries, and we're leading the charge. Genpact's AI Gigafactory, our industry-first accelerator, is an example of how we're scaling advanced technology solutions to help global enterprises work smarter, grow faster, and...

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 Organization is a well-established name in consulting and advisory.Job Summary:Strategic Affairs is a dynamic, proactive professional responsible for supporting the firm in myriad non-client domains, and driving strategic initiatives related to knowledge management, institutional rankings, academic research, and social media presence.This role...