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Ambu A/S
13d ago

Software Project Manager(m/w/x)

Augsburg
Full-timeOn-siteExperienced
AI/ML

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.

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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

Bachelor's degree
OR
Master's degree

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

JiraConfluenceMS Project

Languages

EnglishBusiness Fluent

Benefits

Learning & Development

  • Personal development opportunities

Other Benefits

  • Wide range of employee benefits
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