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Software Project Manager(m/w/x)
Description
In this role, you will manage complex software projects from concept to market launch, collaborating with diverse teams to ensure compliance with medical device standards while keeping stakeholders informed of progress and risks.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •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 or healthcare technology industry, or other regulated industry
- •Proven track record working 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 an 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 in a company with a strong legacy in physical products
- •Excellent interpersonal skills
- •Exceptional stakeholder management and communication skills (both 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
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Lead end-to-end project management of software development initiatives
- •Plan and manage project timelines, deliverables, dependencies, and risks
- •Collaborate with marketing, engineering, quality, regulatory, clinical, and product development teams
- •Ensure compliance with medical device standards like ISO 13485 and FDA 21 CFR Part 820
- •Oversee the software development lifecycle, including requirements definition and design
- •Drive alignment across business units and manage internal and external stakeholders
- •Communicate progress, risks, and mitigations to executive stakeholders and teams
- •Ensure documentation and traceability meet regulatory and audit requirements
Tools & Technologies
Languages
English – Business Fluent
Benefits
Learning & Development
- •Personal development opportunities
Other Benefits
- •Wide range of employee benefits
- AmbuFull-timeOn-siteSeniorAugsburg
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Software Project Manager(m/w/x)
The AI Job Search Engine
Description
In this role, you will manage complex software projects from concept to market launch, collaborating with diverse teams to ensure compliance with medical device standards while keeping stakeholders informed of progress and risks.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •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 or healthcare technology industry, or other regulated industry
- •Proven track record working 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 an 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 in a company with a strong legacy in physical products
- •Excellent interpersonal skills
- •Exceptional stakeholder management and communication skills (both 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
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Lead end-to-end project management of software development initiatives
- •Plan and manage project timelines, deliverables, dependencies, and risks
- •Collaborate with marketing, engineering, quality, regulatory, clinical, and product development teams
- •Ensure compliance with medical device standards like ISO 13485 and FDA 21 CFR Part 820
- •Oversee the software development lifecycle, including requirements definition and design
- •Drive alignment across business units and manage internal and external stakeholders
- •Communicate progress, risks, and mitigations to executive stakeholders and teams
- •Ensure documentation and traceability meet regulatory and audit requirements
Tools & Technologies
Languages
English – Business Fluent
Benefits
Learning & Development
- •Personal development opportunities
Other Benefits
- •Wide range of employee benefits
About the Company
Ambu A/S
Industry
Healthcare
Description
Ambu ist ein international führendes Medizintechnikunternehmen, das sich auf die Verbesserung der Patientensicherheit und Effizienz im klinischen Alltag konzentriert.
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