Regulatory Affairs Specialist - Tuttlingen, Deutschland - Barrington James
Beschreibung
Tuttlingen, Germany- JOB TYPE
- Permanent
- EMP TYPE
- Full-Time
- EXPERTISE
- QA / RA
- SALARY TYPE
- Annually
- SALARY
- Negotiable
In this role, you will be responsible for a variety of tasks related to the creation and maintenance of technical documentation in compliance with (EU) 2017/745 regulations.
You will also coordinate and evaluate product tests, collaborate with laboratories, and assist with product registration processes on a national and international level.
Requirements:
- You should have a completed scientific or life science degree, preferably in Medical Technology, Mechanical Engineering, or a related field (postgraduate studies are desirable).
- We require 1 to 3 years of professional experience in regulatory affairs specifically within the medical technology industry.
- Exceptional proficiency in both spoken and written German and English is necessary (knowledge of additional languages is considered a plus).
- Demonstrate a meticulous and independent working style that showcases attention to detail.
- Strong teamwork skills and effective communication abilities are essential.
What we offer:
- 30 days of annual leave for a healthy worklife balance.
- As part of our corporate benefits, you will have access to exclusive employee offers.
- We offer a company bike leasing program, allowing you to conveniently commute.
- Participate in various team events held throughout the year, promoting a positive team spirit.
- Excellent prospects for personal and professional development are provided.
- Flexible working hours and parttime options are available to support your worklife balance.
- Join a longterm and secure employment opportunity within a forwardthinking group of companies in the respected medical industry.
- Experience an attractive and professional working environment with streamlined decisionmaking processes.
LI-TH2
LH-REMOTE
Consultant
- Thomas Hatfield
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