LivaNova
80331 München - Deutschland
Wirtschaftsingenieur/in
Arbeit
Teilzeit Abend
ab 20.02.2026
Beschreibung
## General Responsibilities
Project Initiation, Planning, Execution and Monitoring, Closing
- Define project scope, objectives, deliverables, and success criteria in collaboration with stakeholders
- Planning, execution, monitoring of software and hardware new product development projects for medical devices using a hybrid approach, integrating agile methodologies for software innovation and waterfall frameworks for hardware development
- Develop comprehensive project plans, encompassing timel... weiter lesen
Project Initiation, Planning, Execution and Monitoring, Closing
- Define project scope, objectives, deliverables, and success criteria in collaboration with stakeholders
- Planning, execution, monitoring of software and hardware new product development projects for medical devices using a hybrid approach, integrating agile methodologies for software innovation and waterfall frameworks for hardware development
- Develop comprehensive project plans, encompassing timel... weiter lesen
## General Responsibilities
Project Initiation, Planning, Execution and Monitoring, Closing
- Define project scope, objectives, deliverables, and success criteria in collaboration with stakeholders
- Planning, execution, monitoring of software and hardware new product development projects for medical devices using a hybrid approach, integrating agile methodologies for software innovation and waterfall frameworks for hardware development
- Develop comprehensive project plans, encompassing timelines, budgets, and resource allocation
- Monitor project progress, identify and manage risks, and implement contingency plans to ensure objectives are met
- Plan and monitor assigned budget
- Ensure adherence to design controls and product development processes
Cross-functional collaboration
- Ensure effective identification and communication of goals, progress, risks and issues
Regulatory and Compliance Oversight
- Ensure all project activities adhere to medical device regulatory requirements (e.g. ISO 13485)
- Maintain documentation in compliance with quality management systems
## Skills and Experience
- Bachelor’s degree in engineering, Business, or related field
- Project Management Expertise: some years managing end-to-end product development projects in the medical device industry is a "must"
- SW Project Management Knowledge: Familiarity in project management of Medical Device Software (according to IEC 62304)
- Regulated Industry Knowledge: Familiarity with product development processes, including design controls, in compliance-driven environments
- Collaboration & Communication: Strong interpersonal and motivational skills to foster teamwork and alignment across functions and levels
- Problem-solving: Resilience, adaptability, and a proactive approach to navigating challenges
- Technical Proficiency: Experience with project management methodologies (e.g., Agile, Waterfall) and tools like MS Project or similar platforms
- Prior experience in product development or engineering within the medical device industry
- Basic understanding of medical device standards and regulations
- PMP certification is desirable
- Scrum Master experience is desirable
- Fluent English language skills, written and spoken
## What we can offer you
In addition to providing you with a supportive, inclusive and collaborative environment where you will feel empowered to take ownership and drive meaningful change, we will reward you with the following:
- A dynamic role in an advanced Medical Device environment interfacing with all worldwide regulatory landscapes supporting your professional career growth
- Exposure to a *State-of-the-Art* medical device development process, in close co-operation with international clinicians
- Competitive base salary
- Variable short-term & long-term incentives
- Recognition: through our STARS Program, we recognize and celebrate our colleagues’ contributions and achievements
If you like the sound of the above and feel energized by the idea of joining a great brand at a moment of exciting expansion, please apply now. We look forward to hearing from you!
Project Initiation, Planning, Execution and Monitoring, Closing
- Define project scope, objectives, deliverables, and success criteria in collaboration with stakeholders
- Planning, execution, monitoring of software and hardware new product development projects for medical devices using a hybrid approach, integrating agile methodologies for software innovation and waterfall frameworks for hardware development
- Develop comprehensive project plans, encompassing timelines, budgets, and resource allocation
- Monitor project progress, identify and manage risks, and implement contingency plans to ensure objectives are met
- Plan and monitor assigned budget
- Ensure adherence to design controls and product development processes
Cross-functional collaboration
- Ensure effective identification and communication of goals, progress, risks and issues
Regulatory and Compliance Oversight
- Ensure all project activities adhere to medical device regulatory requirements (e.g. ISO 13485)
- Maintain documentation in compliance with quality management systems
## Skills and Experience
- Bachelor’s degree in engineering, Business, or related field
- Project Management Expertise: some years managing end-to-end product development projects in the medical device industry is a "must"
- SW Project Management Knowledge: Familiarity in project management of Medical Device Software (according to IEC 62304)
- Regulated Industry Knowledge: Familiarity with product development processes, including design controls, in compliance-driven environments
- Collaboration & Communication: Strong interpersonal and motivational skills to foster teamwork and alignment across functions and levels
- Problem-solving: Resilience, adaptability, and a proactive approach to navigating challenges
- Technical Proficiency: Experience with project management methodologies (e.g., Agile, Waterfall) and tools like MS Project or similar platforms
- Prior experience in product development or engineering within the medical device industry
- Basic understanding of medical device standards and regulations
- PMP certification is desirable
- Scrum Master experience is desirable
- Fluent English language skills, written and spoken
## What we can offer you
In addition to providing you with a supportive, inclusive and collaborative environment where you will feel empowered to take ownership and drive meaningful change, we will reward you with the following:
- A dynamic role in an advanced Medical Device environment interfacing with all worldwide regulatory landscapes supporting your professional career growth
- Exposure to a *State-of-the-Art* medical device development process, in close co-operation with international clinicians
- Competitive base salary
- Variable short-term & long-term incentives
- Recognition: through our STARS Program, we recognize and celebrate our colleagues’ contributions and achievements
If you like the sound of the above and feel energized by the idea of joining a great brand at a moment of exciting expansion, please apply now. We look forward to hearing from you!
Ref-Nr.: 9440365
Aktualisiert:
23.02.2026
Quelle: Bundesagentur für Arbeit
weitere Infos Rechtliche Hinweise zur Nutzung
Ob die Stelle noch verfügbar ist und weitere Informationen findest du direkt auf der Website der Bundesagentur für Arbeit. Bitte beachte: OPROMA ist nicht der Anbieter dieser Stelle und kann keine Auskünfte geben.
weitere Infos Rechtliche Hinweise zur Nutzung
Ob die Stelle noch verfügbar ist und weitere Informationen findest du direkt auf der Website der Bundesagentur für Arbeit. Bitte beachte: OPROMA ist nicht der Anbieter dieser Stelle und kann keine Auskünfte geben.
Passende Jobvorschläge
Basierend auf Beruf und Standort
Basierend auf Beruf und Standort
Passende Jobs für dich
Birkenstock Group B.V. & Co. KG
Köln
Feste Anstellung
CANCOM SE
Frankfurt am Main, Jettingen-Scheppach, Stuttgart
Feste Anstellung
BWT Pharma & Biotech GmbH
Bietigheim-Bissingen
Feste Anstellung
JTJ Sonneborn Industrie GmbH
99869 Sonneborn
Feste Anstellung
Kostenlose Hilfe für deine Bewerbung
Erstelle ein kostenloses Bewerberprofil und erhalte unser E-Book
"Die perfekte Bewerbung" – plus weitere Vorteile für deine Jobsuche.
Gratis E-Book: Die perfekte Bewerbung
Werde von Arbeitgebern gefunden
Passende Jobvorschläge nach Beruf & Stadt
Jobs speichern & später bewerben
Kostenlos & unverbindlich - Keine Werbung - Account jederzeit löschbar
Die Bewerbung erfolgt über die Webseite der Bundesagentur für Arbeit (BA).
