Licensing & Regulatory Affairs Executive

Supporting the RA-FDF Team and contributing in the regulatory activities in order to achieve the objectives of the department which are:  obtaining global approval for CENTRIENT products, including the lifecycle management of the registration dossiers according to business planning.Key Individual AccountabilitiesCollection of information and preparation of...

Additional Locations:N/ADiversity - Innovation - Caring - Global Collaboration - Winning Spirit - High PerformanceAt Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools,...

QA/RA role for medical devices. Handle regulatory docs, QMS, audits, CAPA, risk files, ISO 13485, ISO 14971, and compliance tasks. Support licensing, submissions, tech files, and product approvals. Ensure quality, safety, and regulatory alignment.

Job PurposeWe are seeking a detail-oriented and proactive Regulatory Affairs Specialist to support global regulatory submissions and lifecycle management for pharmaceutical products. The ideal candidate will have hands-on experience with CTD/eCTD documentation, regulatory compliance, and dossier preparation, particularly for US Markets.Key...

Job PurposeWe are seeking a detail-oriented and proactive Regulatory Affairs Specialist to support global regulatory submissions and lifecycle management for pharmaceutical products. The ideal candidate will have hands-on experience with CTD/eCTD documentation, regulatory compliance, and dossier preparation, particularly for Canada Markets.Key...

Responsibilities:* Prepare regulatory dossiers for product approvals* Collaborate with cross-functional teams on dossier updates* Ensure compliance with drug regulations according to NAFDAC standards.* Manage LOAs, COAs & BDNAF submissions

Manager – Aeropolitical AffairsReporting to: Senior Manager – Aeropolitical & Industry AffairsThe Manager – Aeropolitical Affairs will be responsible for supporting the Department in expanding traffic rights and market access for IndiGo and will also be responsible for ensuring adherence to regulatory requirements as required to expand and maintain...

About NothingNothing exists to make tech feel exciting again.We're building a different kind of technology company, one that puts design, emotion, and human creativity at the heart of everything we do. From the way our products look and feel to how we communicate and show up in culture, we believe technology should make you feel something.Founded in London...

Job PurposeThe Asst. Manager – Regulatory Affairs (GHC/KSA) will lead regulatory strategy, submissions, and compliance for pharmaceutical products intended for the ROW markets. This is an onsite role based in Gurgaon. The individual will serve as a key regulatory liaison, ensuring products meet all regulatory requirements, supporting lifecycle management,...

Position: AVP- Head -Global In-Licensing and M&ADepartment: Business DevelopmentLocation: GurgaonQualification: B Pharm/M Pharm with MBAYears of Experience: Minimum 10+ years of experience in business development in pharma sector, with emphasis on Licensing of ProductsSummary Of The Overall Job:As General Manager Licensing & Mergers & Acquisitions (M&A), the...