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. As a leading ecosystem, we aim to enable excellent healthcare support for all patients worldwide.

How do we do that?

People are at the center of everything we do!

We connect all players in the healthcare system to ensure patients receive the right therapy, at the right time, and to the right extent—always with the patient's consent and commitment.

Myoncare collects clinical patient data via audited blockchain, without accessing the data directly, and ensures security through encryption. For the first time, all patient care functions—previously isolated or incomplete—are integrated into a single application!

We have ambitious plans for today and the future! That’s why we seek innovators, change-makers, and minds ready for new challenges.

Talent and commitment are key. Join us and help realize our mission.

Myoncare offers a space to develop your problem-solving skills, grow professionally, and work on meaningful projects where you can truly make an impact.

Experience the digital revolution in healthcare firsthand as our new

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

Tasks

We are seeking an experienced Technical Project Manager (f/m/d) to lead cross-functional projects within our product development lifecycle. This role will coordinate releases, ensure regulatory compliance (ISO 13485, MDR), and foster 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 communication between product, engineering, and quality teams
• Track progress, manage risks, and ensure milestones are met
• Prepare and maintain technical documentation, including DHFs and risk management files
• Support audits and regulatory inspections as needed

Requirements

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

Nice-to-Have:

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

Soft Skills

• Team-oriented and reliable character
• Problem-solving attitude
• Good communication skills
• Fluent in English (verbal and written)
• Analytical thinking
• Strong organizational skills

Benefits

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

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

Become part of the ONCARE family. Apply today with your complete application, including your earliest start date and salary expectations.

We look forward to hearing from you!

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