Regulatory Affairs Manager for Medical Devices - East Dublin, United States - Cascade Industries

Description

What can you expect?

• You will create and maintain the necessary documentation for the approval of medical devices (focus on endoscopy / spine) in international markets
• You will monitor international regulatory requirements and market-specific registration requirements
• You will implement regulatory requirements in coordination with internal process owners from R&D, product management, and sales
• You will handle change and renewal procedures as well as maintain existing registrations
• You will communicate closely with external agencies and authorities worldwide and continuously develop and improve processes

What do we offer?

• Become an Endoscopic.Spine.Expert. with the help of our own joimax ESPINEA Academy. Great colleagues support individual training, promote and challenge the achievement of common goals, and are not afraid to go against the current
• The right benefits count - whether it's fresh fruit and drinks, offers from the Corporate Benefits program for private shopping at home, or the flexible, rechargeable prepaid credit card for daily life
• Turbulent times? We provide security with our offers for retirement provision, group accident insurance, and company savings plans
• Long-term and sustainable - this is how we plan with you, including an attractive salary, 30 days of annual leave (for a full-time position), an unlimited employment contract, and flexible working hours