Level: Lead

Job Field: Application, Project

Employment Type: Full Time

Contract Type: Permanent employment

Salary: from 68.000 € Gross/Year

Location: Neukirchen an der Vöckla

Working Model: Hybrid, Onsite

Job Summary

In this role, you will lead medical software projects, overseeing development, validation, and release processes while ensuring compliance with relevant regulations and maintaining clear communication across teams.

Your role in the team

Lead and manage medical software projects from concept through development, validation, and release.
Plan, coordinate, and monitor project timelines, budgets,, and resources.
Ensure compliance with applicable medical device regulations and standards (e.g. IEC 62304, ISO 13485, ISO 14971).
Act as the primary interface between software development, quality management, regulatory affairs, and external partners.
Identify project risks and implement mitigation strategies.
Track project progress and report status to stakeholders and management.
Ensure proper documentation throughout the entire software lifecycle.

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Our expectations of you

Education

Degree in Computer Science, Software Engineering, Biomedical Engineering, or a related field.

Qualifications

Solid understanding of medical software development lifecycles and regulatory requirements.
Excellent communication and stakeholder management skills.
Ability to coordinate cross-functional teams and external suppliers.
Structured, goal-oriented, and reliable working style.
Excellent written and verbal communication skills in German and English.

Experience

Proven experience in managing software projects within the medical device or regulated environment.
Starke Projektmanagementfähigkeiten und Erfahrung mit relevanten Methoden (z. B. Agile, Waterfall oder hybride Modelle).

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