National Regulatory Affairs Specialist - Oakwood, GA, United States - Titan Industries
Description
The advertised workplace (Aschau, Erfurt or remote) will be discussed based on the applicant's place of residence. The training will take place over 6 weeks at the main location.Your responsibilities - challenging:
- Support in implementing MDR 2017/745, related guidelines and standards
- Creation and maintenance of technical documentation for existing products and new developments
- Communication with relevant regulatory authorities and notified bodies
- Support in conducting conformity assessment procedures
- Assistance in creating and developing sales support materials (product brochures, etc.)
- Close collaboration with adjacent departments
Your qualifications - qualified:
- Previous experience in the medical technology field, as well as project management experience, is advantageous
- Basic knowledge of medical technology standards
- Strong customer orientation
- Pragmatic, analytical and structured approach to work
- Confident and assertive demeanor
- High motivation, flexibility and team spirit
- Enjoyment in learning new skills and competencies
We offer - attractive:
As a secure employer, we support our Königsee employees with many opportunities and flexible options for all stages of life
Discover us:
- Structured and comprehensive training at our company locations, with a mentor by your side
- Varied and responsible tasks with short decisionmaking processes and a flat hierarchy
- A secure and permanent position in a growing company
- Worklife balance through familyfriendly and social personnel policies, including flexible working hours
- Sustainability and responsibility
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