Shape the transition from reactive quality assurance to proactive, data‑driven quality prevention.
As part of the strategic transformation program Automated Infusion Systems (AIS) First in Quality, B. Braun aims to strengthen and modernize quality processes across the entire product lifecycle. As a Project Manager (f/m/d), you will lead this ambitious initiative and play a key role in advancing quality standards, cultural evolution, and digital transparency.
Responsibilities:
1. Project leadership with clarity and control
You assume full responsibility for planning, executing, and monitoring the AIS First in Quality project. You lead an interdisciplinary project team across Quality, R&D, Operations, Service, IT, and Data Analytics.
You develop a clear project structure, define governance processes, and establish transparent communication channels. In addition, you ensure clear roles, responsibilities, and decision rights.
You foster cross‑functional collaboration, actively remove roadblocks, and manage timelines, risks, and budget. With transparent reporting and structured change management, you ensure smooth project execution.
2. Translating strategic goals into tangible results
You derive concrete measures, work packages, and measurable outcomes from the transformation strategy “from reaction to prevention.”
You ensure alignment between digital PLM concepts, such as Single Source of Truth, lifecycle transparency, and analytics and operational requirements
Through consistent prioritization, you prevent fragmented activities and maintain focus on high‑impact results. You also coordinate the project with related digital and quality‑driven initiatives.
3. Driving data‑based quality and cultural change
You actively support the cultural shift toward data excellence, transparency, and proactive quality thinking.
Together with the Data Analyst, you develop meaningful KPIs, central dashboards, and data‑driven control mechanisms.
You ensure that data is used not only retrospectively but especially as a basis for preventive quality decisions.
You also support lifecycle benchmarking, identify improvement levers, and engage key stakeholders through structured communication.
Professional Qualifications:
Degree in Industrial Engineering, Mechanical Engineering, Medical Technology, or a comparable technical field; alternatively, a business or quality‑focused degree with a technical orientation.
Several years of experience leading cross‑functional transformation projects.
Strong expertise in quality assurance and regulated environments.
Knowledge or certifications in quality management, e.g., ISO 9001 Auditor, ISO 13485 Auditor, DGQ or TÜV qualifications.
Preferred Qualifications:
Project management certifications such as IPMA Level C/D, GPM, PMI PMP/CAPM, or PRINCE2 Practitioner
Experience with structured problem‑solving methods such as Six Sigma, Lean Management, FMEA, or Root Cause Analysis
Experience with digital PLM systems (e.g., Teamcenter, Windchill) as well as ERP and QMS systems (e.g., SAP, TrackWise)
Understanding of regulated industries, especially medical devices, and familiarity with the relevance of traceability and compliance (e.g., EU MDR, FDA, ISO 13485)
Personal Competencies:
Excellent communication and leadership skills, including negotiation capability
Ability to summarize complex technical matters in a clear written format and present them effectively
Structured and analytical working style combined with strong conceptual abilities
Independent working approach, resource awareness, and a pragmatic mindset
Benefits:
Company pension scheme
Mobility benefits such as the B. Braun job ticket or job bike
Employee discounts
Various working models (e.g., job sharing, part‑time)
B. Braun Avitum AG | Tobias Franke | +495661715253