Freiburg Area - GRA - 30 Vacation Days

What you can enjoy:

• An easy-going and pleasant workday: In your assigned tasks, you will establish close cooperation with other departments, including R&D and Production. Since both areas are in-house, communication is fast and transparent.
• Strong work-life balance: Supported by several conditions such as flexible working hours, compensation for overtime, and 30 vacation days.
• Internal development opportunities: The average employee retention in the RA department is approximately 7+ years.

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!