Job Description: JOB SUMMARY: The Regulatory Affairs Specialist is responsible for planning, preparing, coordinating, and managing global regulatory submissions and registrations for medical devices, including US 510(k), EU technical documentation, and international dossiers. The role represents
Company Description International Medical Industries, Inc. (IMI) is a long-established leader in tamper-evident technologies for IV syringes, oral dispensers, and other delivery systems. For over 40 years, IMI has provided innovative products to admixture, compounding, and
Regulatory Affairs Specialist The Regulatory Affairs Specialist is responsible for planning, preparing, coordinating, and managing global regulatory submissions and registrations for medical devices, including US 510(k), EU technical documentation, and international dossiers. The role represents Regulatory
Principal Regulatory Affairs Specialist As 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 our state-of-the-art Ultrasound
VP Global Quality And Regulatory Trelleborg Medical Solutions is seeking a VP Global Quality and Regulatory, based from their Minneapolis MN headquarters. As a valued team member with Trelleborg, you will enjoy: Competitive compensation: $220,000-225,000 +