We are seeking a detail-oriented Project Coordinator to support our Global Regulatory Services team. This role offers a unique opportunity to contribute to important regulatory submissions while collaborating with various teams across the organization.

Responsibilities

• Manage and track the status of EU MDR and international regulatory submissions.
• Coordinate administrative activities and maintain accurate records across multiple teams.
• Create metrics and reports to measure the progress of submissions.
• Establish and nurture relationships with international regulatory and business unit affiliates.
• Provide regular status updates and communications to ensure timely submissions.
• Train international affiliates on proper system usage and documentation.

Skills

• Excellent communication and collaboration skills to work effectively with diverse teams.
• Strong attention to detail and organizational abilities for accurate documentation and reporting.
• Proficient in tracking and managing multiple projects simultaneously.

Preferred Skills

• Background in Quality, Regulatory, or Biomedical fields is advantageous.
• Experience with medical devices is a plus but not mandatory.

At Horizontal, we are committed to fostering a diverse and inclusive work environment where all individuals feel valued and empowered. We welcome applicants from all backgrounds to apply and contribute to our mission.

By applying for this position, you acknowledge and agree that Horizontal Talent may contact you regarding your application using automated technology, including phone calls, SMS/text messages, or email, which may be delivered by our virtual AI recruiter, Alex.