Technical Project Manager (f/m/d) - Medical Software

We are status quo breakers, game changers and pathway makers!

With our health platform myoncare, we are transforming the healthcare market and, as a leading ecosystem, we want to enable excellent healthcare support for all patients in the world.

How do we do that?

People are at the center of everything we do!

We connect all the players in the healthcare system to ensure that patients receive the right therapy, at the right time and to the right extent. All with the commitment and consent of the patient.

Myoncare collects clinical patient data thanks to audited blockchain, without its own access, and ensures its security through encryption. For the first time, all patient care functions that previously existed as individual solutions or in incomplete form are bundled into one application!

We have big plans - today and tomorrow! And that's why we are looking for innovators, change-makers and minds that are ready to take on new challenges.

Talent and commitment are the key and that's why we need YOU! Come join the team and help us realise our mission.

Myoncare offers you a space to flex your problem-solving muscles, develop and expand your skills and work on projects that really matter so you can grow with us.

Experience the digital revolution of the healthcare system first hands as our new

Technical Project Manager (m/f/d) - Medical Software.

We are seeking an experienced Technical Project Manager (f/m/d) to lead cross-functional projects within our product development lifecycle. This role will be pivotal in coordinating releases, ensuring regulatory compliance (ISO 13485, MDR), and driving collaboration across engineering, QA, and regulatory teams.

Key Responsibilities:

• Lead and manage software development projects from planning to release
• Oversee release management processes, ensuring timely and compliant software delivery
• Coordinate ISO 13485 and MDR documentation efforts with QA/RA teams
• Facilitate cross-functional communication between product, engineering, and quality teams
• Track progress, manage risks, and ensure alignment with project milestones
• Prepare and maintain technical project documentation, including DHFs and risk management files
• Support audits and regulatory inspections as needed

• Degree in Computer Science, Engineering, or related field
• 3+ years of experience in project management within a regulated (medical or life sciences)software environment
• Solid knowledge of ISO 13485 and EU MDR documentation requirements
• Proven experience in release management in agile or hybrid environments
• Excellent organizational and communication skills
• Fluent in German (C1+) and English (C1+)

Nice-to-Have:

• Certified PMP, IPMA, or equivalen
• Experience with tools like Jira, Confluence, and medical QMS systems
• Familiarity with risk management (ISO 14971

Soft skill requirements:

• Team oriented and reliable character
• Problem solving attitude
• Good communication skills
• Fluent in English (verbal and written)
• Analytic thinking
• Organizational skills

• Competitive salary with performance-based growth
• Central located office with plenty of lunch options
• Personalized onboarding experience
• Global team shaping the future of healthcare
• Team events
• Coffee and tea stations for daily recharge
• Employee discounts
• Networking opportunities with sister companies (sqanit & CONVIEN) for professional growth

Contribute to the digitalization of healthcare and take visionary step into the future with us!

Become part of the ONCARE family and apply today with your complete application documents, stating your earliest possible starting date and your salary expectations.

We are looking forward to hearing from you!

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