
Regulatory Affairs Officer
4 days ago
- Prepare, review & submission of quality regulatory dossiers in CTD/eCTD format for Europe & other domestic markets.
- Support product development, registration, & lifecycle management in Europe
- Manage Regulatory Compliance & Approvals
Required Candidate profile
- Minimum 4 years of exp in Formulation OSD
- Willing to work in Chennai
3.Strong expertise in EU, EMA, MHRA & other international regulatory framework - Exposure in domestic regulatory market
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Regulatory Affairs
7 days ago
Chennai, Tamil Nadu, India ABABIL HEALTHCARE Full time ₹ 5,00,000 - ₹ 10,00,000 per yearJob Description Role - Regulatory Affairs - Medical DevicesExperience - 1 to 3 YearsLocation- Madhavaram, ChennaiBudget - As per the industryKey Responsibilities:1. Regulatory Submissions: Prepare and submit regulatory documents to authorities for approval, such as new product applications, amendments, and supplements.2. Compliance: Ensure products meet...
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Regulatory Affairs Executive
7 days ago
Chennai, Tamil Nadu, India Medopharm Full time ₹ 9,00,000 - ₹ 12,00,000 per yearJob Description: Regulatory Affairs Executive (ROW Markets)Industry: PharmaceuticalsExperience: 3-5 YearsLoaction: ChennaiKey Responsibilities:Dossier Submissions: Compile & submit ACTD, CTD, and country-specific dossiers for ROW markets.Regulatory Queries: Prepare and respond to health authority queries on submitted dossiers.Document Review: Review BMR,...
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Regulatory Affairs Professional
1 week ago
Chennai, Tamil Nadu, India beBeeRegulatoryAffairs Full time ₹ 1,04,000 - ₹ 1,30,878Regulatory Affairs SpecialistThis is a key role within our organization, responsible for ensuring compliance with regulatory requirements. The Regulatory Affairs Specialist will work closely with cross-functional teams to prepare and submit amendments and supplements for assigned products.Key Responsibilities:Amendment and Supplement Preparation: Prepare,...
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Regulatory Affairs Opportunities
3 days ago
Chennai, Tamil Nadu, India beBeeRegulatoryAffairs Full time ₹ 9,00,000 - ₹ 15,00,000Regulatory Affairs Opportunities">Candidates seeking a challenging role in regulatory affairs will find this position appealing.The ideal candidate will be responsible for preparing and submitting regulatory documents, including new drug applications (NDAs) and annual reports. Additionally, they will manage US FDA registration activities and oversee the...
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Regulatory Affairs Specialist
14 hours ago
Chennai, Tamil Nadu, India beBeeRegulatoryAffairs Full time ₹ 15,00,000 - ₹ 20,00,000Regulatory Affairs Role in Pharma Industry">Candidates should review and prepare regulatory submissions, including new filings and amendments to Annual reports. This includes reviewing of DMF for USFDA registration activities. ">Key Responsibilities">1. Review and preparation of regulatory submissions2. Management of DMF and USFDA registration activities...
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Regulatory Affairs Associate
5 days ago
Chennai, Tamil Nadu, India RegTrac Full time ₹ 9,00,000 - ₹ 12,00,000 per yearCompany OverviewRegTrac is a leading healthcare regulatory partner specializing in Global Regulatory Affairs, Quality Systems, and Compliance for Medical Devices, Cosmetics, and Consumer Products. With expertise in navigating regulatory requirements across diverse markets, RegTrac empowers MedTech companies to innovate and expand globally while ensuring...
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Chennai, Tamil Nadu, India Morulaa Healthtech Full time ₹ 5,00,000 - ₹ 8,00,000 per yearJob Title: Senior Regulatory Affairs Team Lead Medical DevicesLocation: Chennai, IndiaDepartment: Regulatory AffairsExperience Required: Minimum 5 yearsReports To: Head of Regulatory Affairs / Director of Quality & RegulatoryJob Summary:We are seeking a highly skilled and experienced Senior Regulatory Affairs Team Lead to manage and lead our regulatory...
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Chief Regulatory Affairs Specialist
3 days ago
Chennai, Tamil Nadu, India beBeeRegulatory Full time ₹ 9,60,000 - ₹ 12,00,000Regulatory Affairs PositionManage regulatory submissions, including new drug applications (NDAs), complete response letters (CRLs), information requests (IRs), and amendments to existing NDAs.File post-approval and prior approval supplements in compliance with FDA regulations.Review change controls to assess their impact on regulatory alignment and ensure...
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Chennai, Tamil Nadu, India Seven Consultancy Full timeJOB DETAILS Candidates should review and prepare regulatory submissions, including new ANDA filings, amendments and Annual reports to the ANDA.Review of DMF Manages USFDA registration activities FUNCTIONAL AREA Pharma Jobs Consultancy in Chennai, Pharma Jobs Consultancy near me, Pharma Jobs, Top, Best, Jobs Consultancy in Chennai, regulatory affairs jobs...
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Chennai, Tamil Nadu, India Seven Consultancy Full timeJOB DETAILS Manages, reviews, and authors regulatory submissions, including new ANDA filings, complete response letters (CRLs), information requests (IRs), and amendments to existing ANDAs.Responsible for filing Post-Approval and Prior Approval Supplements in compliance with FDA requirements.Reviews change controls to assess regulatory impact and ensure...