Global Device Registration - High-risk class - Breisgau

In this role, you will be responsible for contributing to the creation of technical documentation for existing and new products, as well as implementing the global regulatory strategy. 

You will also handle the registration of high-risk devices, which present significant new challenges to the regulatory managers.

Every day, you will namely advance your knowledge by collaborating with various departments (especially Production and R&D) and by supporting the product development from different perspectives. 

This makes your daily work diverse and interesting, as you learn something new every day.

Your potential employer is a German company, who has been being over 40 years on the market and has several placed products. As a result, every employee can count on great stability, enabling long-term, secure career planning.

Are you feeling interested in principle? Contact me for more information

Your key responsibilities:

• Contributing to the creation of technical documentation for marketed and new medical devices
• Close collaboration with other departments (especially Production and R&D) to ensure efficient product development
• Implementing the global regulatory strategy
• Regular contact with relevant regulatory authorities
• Serving as the point of contact for external stakeholders regarding regulatory matters.

Location: Greater Freiburg area

Type of contract: Permanent position. You will be employed directly by my client.

Start date: As soon as possible

What you bring:

• At least 2 years of global regulatory experience in the medical device industry.
• Good knowledge of German.
• A proactive and curious mindset

My contact details:

Dr. Emma Fleury
Principal Consultant
Pharma und MedTech

+49 (0) 89 38035861

EFleury@i-pharmconsulting.com

Check out the recommendations from my clients and candidates on my LinkedIn profile:

https://www.linkedin.com/in/dr-emma-fleury-023790a2/details/recommendations/?detailScreenTabIndex=0

If your profile does not meet the key requirements of the position, I regret that due to the high volume of applications, I will not be able to provide feedback. In that case, let's try again with the next opportunity!