Head of IT Development (m/f/d)

as a development manager IT (m/w/d) you will lead a team of 5 to 10 developers:inside and introduce the direction for pioneering software solutions in the medical environment the management and further development of the IT development department and the responsibility for the development and support of innovative software solutions for medical devices are in your hands while ensuring and implementing high quality standards, you always keep in mind compliance with all regulatory requirements and error analysis You work closely with large customers and the parent company, analyzes quality problems quickly and introduce appropriate corrective measures in the IT sector responsible for managing and coordinating developers, IT specialists and external service providers You as well as the smooth interface management for production Together with suppliers, you meet the strictest requirements and medical standards and shape the further development of the IT infrastructure for the construction and operation of medical devices compliance with all regulatory requirements (e.g. MDR, data protection), complete documentation and innovation management in the field of software technology for medical devices are key components of your daily work Project progress, budget planning and resource management You independently monitor and continuously improve

You have completed university studies with technical focus in electrical engineering, mechanical engineering, medical technology, physics or computer science relevant experience in product development from concept phase to market launch You also have at least 5 years of experience in the development of active medical devices (Class IIa, IIb) You already have application knowledge in spirometry, ventilation technology or intensive medicine Your experience extends to production processes, production ramp-up and process validation in manufacturing in the field of plastic injection moulding you have proven expertise You have experience in clinical evaluation, post market surveillance and global approval, such as Canada, LATAM, ASEAN, China or India in audits as well as in dealing with FDA inspections well-founded knowledge of measurement and control technology and gas/liquid sensor technology in the creation of product files (MDR, FDA) and in the safe handling of design control and document control you are absolutely routined comprehensive application experiences in MDR (EU 2017/745) and multiannual experience with relevant standards and standards (ISO 13485, ISO 14971, IEC 62304) German and English master fluently, at least on level C1 in word and writing a valid work permit are of course for you

from 30,00€ /hour from the first day safe workplace in a future-proof industry flexible working hours flat hierarchies and short service paths free staff parking Holiday and Christmas money

What you can always rely on persona service: €50 per month for your mobility depending on the location, e.g. for the Deutschlandticket uvm. Premiums and holiday and Christmas money free help for your children on the Ubimaster learning and remedial platform numerous shopping discounts at well-known brands about our corporate program excellent personal support and regular feedback talks wide range of training possibilities