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Leading end-to-end software development for single-use medical devices. Proven track record with EU MDR, FDA, and IEC 62304 required. Personal development opportunities, exciting job challenges.
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Anforderungen
- Bachelor's or Master's degree in Computer Science, Engineering, Life Sciences, or related field
- Proven project management experience in software development in medical device, healthcare technology, or other regulated industry
- Proven track record with medical device regulations (EU MDR, FDA), quality systems (ISO 13485), and software lifecycle standards (IEC 62304)
- Familiarity with Software as a Medical Device (SaMD) and/or AI-based software projects from concept to commercialization
- Mastery of agile methodologies (Scrum, SAFe, LeSS, or similar) and experience in agile-at-scale environment
- Proficiency with project management tools (e.g., Jira, Confluence, MS Project, or similar)
- Open-mindedness and eagerness to drive new software initiatives
- Excellent interpersonal skills
- Exceptional stakeholder management and communication skills (technical and non-technical audiences)
- Great planning, scheduling, and risk management capabilities
- Ability to manage budgets, resources, and priorities across complex projects
- Strong analytical thinking, problem-solving, and decision-making skills
- Flair for fostering collaboration, accountability, and transparency across diverse teams
Aufgaben
- Lead end-to-end project management of software development initiatives
- Ensure delivery on time, within scope, and within budget
- Plan project timelines, deliverables, dependencies, and risks
- Manage project timelines, deliverables, dependencies, and risks
- Report on project timelines, deliverables, dependencies, and risks
- Collaborate with marketing, engineering, quality, regulatory, clinical, and product development teams
- Ensure compliance with medical device standards (ISO 13485, IEC 62304, MDR, FDA 21 CFR Part 820)
- Oversee software development lifecycle
- Manage requirements definition, design, verification/validation, and post-market surveillance
- Drive alignment across business units
- Manage internal and external stakeholders
- Communicate progress, risks, and mitigations to executive stakeholders and cross-functional teams
- Ensure documentation meets regulatory and audit requirements
- Ensure traceability meets regulatory and audit requirements
Berufserfahrung
Ausbildung
Sprachen
Tools & Technologien
Benefits
- Personal development opportunities
- Continuous professional and personal development
- Exciting job challenges
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Zur Originalanzeige bei Ambu A/SÜber das Unternehmen
Ambu ist ein international führendes Medizintechnikunternehmen, das sich auf die Verbesserung der Patientensicherheit und Effizienz im klinischen Alltag konzentriert.
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