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Full-Time
The Principal Regulatory Affairs Specialist works independently in preparing and managing ... Interpret federal/state/international regulations as they apply to Cepheid products, processes and ...
The Principal Regulatory Affairs Specialist works independently in preparing and managing ... Interpret federal/state/international regulations as they apply to Cepheid products, processes and ...
Principal International Regulatory Affairs Specialist (RA QA / Compliance / Health Care / Medical Device) Responsibilities The Principal International RA Specialist will plan and execute global ...
The International Regulatory Affairs Specialist is responsible for supporting a variety of regulatory activities. This includes executing on tasks and deliverables to regulatory project timelines and ...
What You Will Do As the International Regulatory Affairs Specialist, you will have the opportunity to support EUMDR regulatory submissions for medical devices, pharmaceutical products, biocides and ...
Regulatory Affairs Specialist - International US, US, CA - San Diego Minimum Level of Education Required: Bachelors Degree Percentage of Travel: Up to 10% Location: San Diego, CA Ref#: 105337 Share ...
The Regulatory Affairs Specialist II is responsible for supporting the development and ... Prepares international dossiers for EMEA, LATAM, APAC, and other key market affiliates, to obtain ...
The Regulatory Affairs Specialist is responsible for planning and executing global regulatory activities necessary to obtain and maintain regulatory approvals within International Regions. Regulatory ...
The REGULATORY AFFAIRS SPECIALIST - PROJECT LEAD provides support through the product life cycle on ... Established 20 years ago in Europe, our client is an international leader in the development and ...
Overview The Regulatory Affairs Specialist I at Cook Inc. is responsible for the planning and ... Requires occasional early morning or late evening teleconferences International and domestic travel ...
The Sr. Specialist, Regulatory Affairs- Medical Device is a critical role that will include ... Experience with domestic and international regulatory filings, registrations, and product licensing ...
Bio-Rad Laboratories is seeking a Regulatory Affairs Specialist who will support the RA team ... international regulatory compliance in the medical device industry. * Knowledge of FDA and CE Mark ...
The Regulatory Affairs Specialist will work closely with cross-functional staff members to support ... international medical device regulations and submissions * Post-market complaint reporting
The State and Regulatory Affairs Specialist will support SOLV Energy through monitoring and ... A bachelor's degree in political science, law, economics, international relations, or other public ...
SUMMARY The Regulatory Affairs Specialist is responsible for preparing global regulatory ... Travel, both domestic and international, may be required up to 10% of time. RESPONSIBILITIES
Team with business unit Regulatory Affairs Specialists (RAS) and international regulatory staffs to provide regulatory support for new products. Work with RAS, engineers and technical experts to ...
The Position We are hiring a Senior Regulatory Affairs Specialist II who will support clinical ... Prepares international registration dossiers for use in clinical studies and international ...
Remote or Hybrid or Onsite We are currently seeking a Senior Regulatory Affairs Specialist to join ... Determines requirements (local, national, international) and options for regulatory submission ...
What you will do As the Senior Staff Regulatory Affairs Specialist, you will be a recognized ... Evaluate medical device regulations and determine requirements (local, national, international) and ...
SummaryThe Staff Regulatory Affairs Specialist will represent Regulatory Affairs within the ... international regulatory associates to register our devices worldwide. * Authors, prepares, and ...
The Staff Regulatory Affairs Specialist role is a professional position with responsibilities for ... Maintain regulatory intelligence on US and International regulatory requirements related to ...