Regulatory Affairs Specialist Make a meaningful difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex domestic and international regulatory environments. Working in partnership with
Regulatory Affairs Specialist 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
Quality Assurance/Regulatory Affairs Specialist Supports tasks related to Regulatory and Compliance activities including tasks to ensure compliance during product development activities, local, state, federal and any outside US requirements. Supports activities to ensure products consistently meet
Job Title Responsibilities: Prioritize and monitor cases throughout the day, provide status updates as necessary. Support the IVDR labeling conversion and revisions of technical files for appropriate products that are due to convert to the new
For this U.S. based position, the expected compensation range is $178,000 - $213,600 per year, which includes base pay and short-term incentive. The compensation range for this full-time position applies to candidates located within the United
CDD Ready to grow your skills in a supportive, dynamic team and tackle exciting missions in risk prevention and control? Tecno Piemonte Spa is actively recruiting a Technical Specialist - CE Marking & Construction Materials for its headquarters
