Financial Affairs Specialist Jobs in International

The Roles & Responsibilities include;Regulatory StrategyPrepares and submits regulatory submissions according to applicable regulatory requirements and guidelines.Collects and evaluates information on regulatory requirements for quality preclinical and clinical data to meet applic 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...

Primary Function of Position:Partner with the in-country RA team as well as the Product Localization Engineering (PLE) and other cross-functional supporting teams make sure the companys regulatory affairs activities are conducted accurately ethically based upon the latest relevant reg More...

Primary Function of Position:Partner with the in-country RA team as well as the Product Localization Engineering (PLE) and other cross-functional supporting teams make sure the companys regulatory affairs activities are conducted accurately ethically based upon the latest relevant reg More...

Our Work MattersAtKindeva we make products that save lives ensuring better health and well-being for patients around the world. Our Work MattersAs a Regulatory Affairs Specialist at Kindeva your role is essential to ensuring our products remain compliant safe and accessible to patient More...

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected compassionate world.A Day in the LifeJoin our Regulatory Affairs te More...

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...

Our client, a well-established manufacturer with a strong presence in multiple countries, is seeking an experienced Sales Manager to join their UK team. This is an exciting opportunity for a customer-centric professional to play a key role in driving sales performance and enhancing cu 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...