Regulatory Affairs Executive - Remote

Overview

The Regulatory Affairs Executive will be responsible to support and provide guidance to countries in Greater Asia on activities related to EU MDR/IVDR program, ensuring business continuity and collaboration with various stakeholders.

In Short

• Support and guide countries in Greater Asia on EU MDR/IVDR activities.
• Collaborate with regional and global regulatory teams.
• Execute regulatory strategy to enhance partnership and business growth.
• Facilitate and track regulatory submissions.
• Analyze complex regulatory requirements across multiple countries.
• Maintain country registration status and compliance.
• Work on cross-functional activities to expedite market access.
• Contract position with potential for renewal based on performance.
• Prioritize on-site collaboration for creativity and innovation.
• Join a company committed to improving human health.

Requirements

• Experience in Regulatory Affairs, preferably in medical technology.
• Knowledge of EU MDR and IVDR regulations.
• Strong analytical skills for complex problem-solving.
• Ability to collaborate with diverse stakeholders.
• Effective communication skills in English.
• Experience in market access strategies.
• Ability to manage multiple projects simultaneously.
• Understanding of healthcare industry standards.
• Flexibility to adapt to changing regulations.
• Commitment to fostering an inclusive work culture.

Benefits

• Opportunity to work with leading medical technology professionals.
• Career growth and development opportunities.
• Inclusive and rewarding workplace culture.
• Ability to make a significant impact on human health.
• Flexible work arrangements.
• Access to innovative tools and resources.
• Competitive compensation package.
• Supportive leadership team.
• Networking opportunities across global teams.
• Engagement in meaningful work that contributes to healthcare improvements.