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EMEA International Registration Manager

BaltParis, Ile de France, France
On-site Full-time

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Experience Level

Experience

Qualifications

To thrive in this role, candidates should have a strong background in regulatory affairs, particularly in international registration processes. Experience in the medical device industry is preferred. Key qualifications include:Proven experience in regulatory submissions and compliance within EMEA. Strong understanding of medical device regulations and standards. Ability to work collaboratively with cross-functional teams. Excellent communication and organizational skills. Fluency in English; additional languages are a plus.

About the job

About Balt

Balt is committed to enhancing the lives of over 150,000 patients by 2026. Our mission is driven by innovation, collaboration with healthcare providers, and the development of state-of-the-art medical devices.

Our Story

For 45 years, Balt has been at the forefront of medical technology, partnering with physicians and institutions to create sophisticated medical devices. With a presence in 13 offices across 11 countries, we are proud to support healthcare professionals worldwide.

Since introducing one of the first neurovascular intervention devices in 1977, we have grown to offer the most extensive range of medical devices for stroke treatment. As we expand our reach into the peripheral vascular field, our commitment to innovation continues unabated.

We take pride in our mission, our dedicated team, and the remarkable achievements we accomplish together in empowering physicians to save lives.

Why Join Balt? Become a part of a passionate team that is focused on making a real difference in the medical field.

About Balt

Balt is a leading innovator in the medical device sector, specializing in neurovascular and peripheral vascular treatments. With a mission to improve patient outcomes, Balt collaborates closely with healthcare professionals, continuously advancing medical technology to meet evolving needs.

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