Technical Documentation Specialist (m/w/d)

Our client is an internationally leading healthcare company based in Bad Homburg. With high-precision technologies, it makes an essential contribution to global patient care. For an innovative software project in medical technology, we are now looking for qualified reinforcement in the field of verification and technical documentation. The position shall be within the framework of the transfer of workers, fixed to 12 months.

Implementation of the technical verification of a new device software Understanding, applying and implementing technical documentation (document language: English) Creation, maintenance and approval of documents supporting project planning Cooperation in the verification team for quality assurance of medical device software Use and maintenance of automated approval and tracking systems (e.g. Trackwise, Documentum) Creation of status reports and metrics for documentation tracking

Complete technical training (e.g. IT, electronics, mechatronics or comparable) First knowledge of software testing / Quality Assurance (test cases, error logs, tools such as GitLab, Matrix ALM) Very good knowledge of English, especially for technical communication and documentation Good knowledge of German in word and writing Secure handling of MS Office (Word, Excel, PowerPoint), basic knowledge of MS Access of advantage Ideally experience with medical device technology and interfaces (e.g. RS232, CAN) Structured working, analytical thinking and high care Knowledge of regulatory framework conditions (e.g. ISO 13485, IEC 62304, FDA processes) are desirable Teamability, communication strength and readiness to integrate into regulated environments

Attractive working environment with good perspectives Collective pay according to iGZ/DGB rate plus Industry surcharges Personal service and qualified advice Our Employee Benefit Program Orizon PlusPoints Up to 30 days of annual leave JOBV1_EN