Regulatory Affairs Manager

The Regulatory Affairs Associate will manage the preparation, review, and submission of regulatory documents to ensure compliance with applicable regulations. The role will involve monitoring adherence to regulatory requirements, staying updated on relevant guidelines, and providing strategic input on regulatory matters.QualificationsKnowledge of Regulatory...

Job ProfileThe Regulatory Affairs Manager (RAM) for Africa, MENA, and LATAM will lead regulatory strategy, submissions, approvals, and life-cycle management of pharmaceutical, biotech, and nutraceutical products across these diverse regions. The role requires a strong understanding of local health authority requirements, WHO guidance, and international...

Job Role: International Regulatory AffairsResponsible for compilation & submission of Dossier of a generic drug.Hand on experience in Filing dossiers to regulated, emerging and ROW markets.Experienced in CTD/ACTD and Regional Module.Experience in Filing in EU, ASEAN, MIDDLE EAST AND LATAM regions.To obtain approvals for relevant product marketing,...

We're Hiring – Regulatory Affairs Pharmacist | New Delhi Do you want to join a company that is on track to become the No. 1 Oncology & Hematology company in the Philippines next year? If yes, this is your chance.At GetMeds, we believe in more than just medicines. We believe in partnerships, innovation, and building a legacy of accessible, life-saving...

ROLE SUMMARYEnsure Regulatory compliances and handle Government AffairsKEY DUTIES AND RESPONSIBILITIESLegal expertise in Media & Entertainment industry. We prefer a person with experience in Broadcasting sector or who has worked with a Law firm handling Broadcasting issues.Interact and be a bridge between Tata Play and TRAI, MIB, DoT, Industry...

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...

Job Location: DelhiKey ResponsibilitiesPrepare, review, and maintain regulatory documentation (dossiers, registration files, certificates, product information, etc.)Coordinate with sales & marketing team to collect required documents and information for product registrations and submissions.Liaise with the factory regulatory department to ensure timely...

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...

The primary role for the Regulatory Affairs Specialist is to manage end to end Regulatory Submissions & Compliance for Masimo India teamPrepare, draft, and compile 510(k)/any other applicable Premarket Notifications and related FDA submissions.Support domestic and international product filings and registrations, including maintenance of EU Technical Files,...

DescriptionJob Summary : Regulatory Affairs Specialist is responsible for obtaining and documenting our mission-critical, domestic regulatory clearances for Masimo's amazing innovative products. The individual will be the sole RA representative on various project teams for new products.  For each project, the individual will provide regulatory input on,...