Financial Affairs Specialist Jobs in International

DescriptionThe Quality and Regulatory Specialist facilitates and participates in the implementation of the multidisciplinary hospital and system wide Clinical Quality and Patient Safety Performance Improvement Program. This is a healthcare professional who coordinates the planning mon More...

Key Responsibilities: Regulatory Expertise: Manage the regulatory process for Pharmaceutical Finished Formulations across CIS LATAM and Africa.Dossier Management: Compile and review ACTD and CTD dossiers to ensure accuracy and compliance.MOH Query Response: Address and respond to any More...

Responsibilities: This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe support of international product registrations and related regulatory affairs activities including execution of procedures and s More...

Job TitlePrincipal Regulatory Affairs SpecialistJob DescriptionAs a critical member of the Philips Ultrasound- Regulatory Affairs Organization the Principal Regulatory Affairs Specialist will lead and provide regulatory oversight for critical new product development projects ensuring More...

Pour rpondre aux attentes de ce domaine et participer au dveloppement de notre filiale nous recrutons un(e) tudiant(e) en contrat dalternance Assurance Qualit/Affaires Rglementaires partir du 1er septembre 2025.Vous serez rattach(e) au Responsable Affaires Pharmaceutiques et serez ba More...

Additional Information : Due to the nature of our business and the role please note that Intuitive and/or your customer(s) may require that you show current proof of vaccination against certain diseases including COVID-19.  Details can vary by role.Intuitive is an Equal Opportun More...

Responsibilities: Preparing documentation for international regulatory registrations. Preparing technical documentation to compliant to MDD and EU MDR. Defining worldwide regulatory requirements are necessary for regulatory approval of products. Participating in cross functional team More...

Responsibilities: Responsibilities include developing regulatory strategies reviewing design input/output documentation identification of applicable standards and guidance documents performing regulatory assessments to determine the impact of design/process changes preparing regulato More...

Responsibilities: In this role you will perform specialized level work assignments and/or analyses evaluation preparation and submission of documentation for regulatory registration ensuring products and procedures comply with regulatory agency specifications. Supports necessary regu More...

Job Details Los Angeles CA Full Time $85766.00 - $127827.00 SalaryDescription SUMMARY:The Government Affairs Specialist plays a key role in advancing Gracelight Community Healths mission by building strategic relationships with government agencies elected officials and community stake More...

Do you enjoy developing communications managing public engagement and leading digital media strategiesThis role will be primarily responsible for serving as a subject matter expert for public affairs for a federal government client.The position is full time at the client site in Oxnar More...

Additional Location(s):US-CA-Irvine; US-CA-Valencia; US-MA-Marlborough; US-MN-Maple GroveDiversity - Innovation - Caring - Global Collaboration - Winning Spirit- High PerformanceAt Boston Scientific well give you the opportunity to harness all thats within you by working in teams of d More...

Additional Location(s):US-CA-Irvine; US-CA-Valencia; US-MA-Marlborough; US-MN-Maple GroveDiversity - Innovation - Caring - Global Collaboration - Winning Spirit- High PerformanceAt Boston Scientific well give you the opportunity to harness all thats within you by working in teams of d More...

Additional Location(s):US-MN-Maple GroveDiversity - Innovation - Caring - Global Collaboration - Winning Spirit- High PerformanceAt Boston Scientific well give you the opportunity to harness all thats within you by working in teams of diverse and high-performing employees tackling som More...

CK Group are recruiting for a Medical Affairs Team Coordinator, to join a company in the pharmaceutical industry, on a contract basis for 12 months.   Salary:   £20.84 per hour to £27.18 per hour, dependant upon experience.   Medical Affairs Team Coordinator Role:Provide project manag More...

Responsibilities: Preparing documentation for international regulatory registrations. Preparing technical documentation compliant to MDD and EU MDR. Defining worldwide regulatory requirements necessary for regulatory approval of products. Participating on cross functional teams as re More...

IQVIA is The Human Data Science Company focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles IQVIA offers a broad range of solutions that harness advances in healthcare information More...

About Scientia Vascular:Our mission is to save lives. Scientia Vascular is aleading innovator and manufacturer of endovascular medical devices. We usemicromachining and microfabrication processes to manufacture products thatprovide physicians with enhanced performance for optimal outc More...

Key Responsibilities: Regulatory Submissions: Prepare and submit dossiers for product approvals to regulatory authorities (CDSCO CE USFDA etc.). Manage correspondence and follow-ups with regulatory bodies. Compliance Management: Ensure compliance with ISO 13485 MDR and oth More...

Responsibilities: This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe support of international product registrations and related regulatory affairs activities including execution of procedures and More...