TOMTEC IMAGING SYSTEMS GMBH, with headquarter located in Munich / Germany, is a worldwide leader for medical image software solutions. Specialized in cardiology it offers state-of-the-art solutions for clinical customers and industry partners. The products encompass a wide range of 2D and 3D/4D technology for visualization, automated analysis, quantification, reporting and image management. TOMTEC products are available for adult and pediatric cardiology, obstetrics, gynecology, radiology and vascular diagnostics. Moreover, TOMTEC offers a sustainable full-service component in sales and an education program with best-practice sharing among professionals. The company claim "Excellence in Digital Healthcare" represents striving for excellent image and analysis quality, ease-of-use, reproducibility of automated measurements and an all-around service- and education offering. The company maintains close working relationships with many leading universities and research institutes around the world.
In July 2017, TOMTEC became a part of the Philips Ultrasound Business group. However, TOMTEC is continuing its vendor independent product portfolio.
In this role, you have the opportunity to
make product releases successful and to maintain the product portfolio throughout the different versions in the market. You will collaborate closely with the software development team and are responsible for software of unknown provenance as well as post market surveillance.
You are responsible for
Manage upcoming releases by identification of variant, deployment and licensing needs
Part of quality gate to assess impact of changes on upcoming release
Decide on branching strategy for upcoming releases.
Identify and address technical risks for upcoming releases
Control active versions in the market and provide infrastructure for building them
Responsible for completion and configuration of all product deliverables with in the device master record (continuous integration environment)
Own processes related to third party SW management and coordinate the respective post market surveillance activities
Trigger product version termination
Cooperate on the technical implementation with the product security officer and the IT tools specialist
Responsible to moderate, decide on and document best practices for technical release management and the respective ways of working in an agile environment
Cooperate with project management to get a successful release in the market
You are part of
the competence unit clinical products which is responsible to enable for efficient, transparent and regulatory compliant development of a high quality product. The unit acts as an umbrella for the development department platform, clinical applications and reporting/measurements. By addressing the needs of the business unit and customer support it helps to make the product successful in the market. You will report into the Senior Manager Clinical Products.
To succeed in this role, you should have the following skills and experience
Degree in engineering (ideally medical engineering)
3+ years of technical knowledge in (medical) software engineering
Project management skills with scripting skills
Distinct ability to work in a team, ability of getting team alignment
Autonomous, well organized and target-oriented
Strong communication and collaboration skills
Language skills: Grade C in English
In return, we offer
Working in a motivated team
Versatile, challenging tasks in a growing company in an international environment
An innovative environment with the chance to evolve
An excellent working atmosphere with flat hierarchies and short decision makings
An attractive and dynamic salary package, excellent employee benefits and supplementary pension
Flexible trust-based working hours, massages, sports courses, regular team events and much more