Technical Documentation Specialist - Hamburg, Deutschland - Adaptive Life Science

Adaptive Life Science

Geprüftes Unternehmen

Hamburg, Deutschland

vor 2 Wochen

Geschrieben von:

Lena Wagner

beBee Recruiter

Beschreibung

_Passionate about making a difference in the medical technology industry? _

Do you love working with technical documentation, in regulatory affairs or quality management?_
We want to hear from you_

Overview:

My client is a leading manufacturer and supplier of high quality ENT treatment units and diagnostic devices for hospitals and private practices, with active customer contacts in over 40 countries.

Tasks:

Create, update, and maintain Technical Documentation for medical devices following MDR guidelines
Contribute to the design, development, and implementation of new products from a regulatory perspective
Conduct regulatory reviews of existing products and assist service providers with product changes
Perform tests on various devices to ensure compliance and approval

Your Profile:

Degree in medical technology, regulatory affairs, or related field
Familiarity with relevant standards such as MDR, ISO , ISO 1497
Experience in creating and maintaining Technical Documentation for medical devices
Background in developing medical devices
Proficiency in CAD software (e.g. SolidWorks)
Good knowledge of MS Office suite
Fluent in both spoken and written German and English (B2+ level)
Resultoriented team player with the ability to work independently and proactively