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Manager NPI Engineering(m/w/x)
Driving design transfer for life-saving mechanical circulatory support devices, leading a team of up to 8 engineers at a global medical device manufacturer. 5+ years MedTech experience, 3+ years people leadership, and strong regulatory knowledge (ISO13485/FDA21CFR820/MDR/GMP) required. Team building focus, cross-site coordination.
Anforderungen
- Master’s degree in science or engineering
- Minimum 5 years’ experience in NPI, industrialization, or product creation
- Minimum 5 years in MedTech or pharma
- Strong knowledge of ISO13485/FDA21CFR820/MDR/GMP
- Minimum 3 years of people leadership
- Strong project management experience (cross-functional and multi-site)
- Excellent communication skills
- Fluent English (negotiation level)
- Further education in business, project management, or leadership
- Fluent German
- Experience in fast-paced, regulated environments
- Structured, analytical mindset and collaborative working style
- Openness to diverse cultures and ways of working
Aufgaben
- Build an NPI team of up to 8 engineers
- Lead an NPI team of up to 8 engineers
- Define design transfer work packages compliant with procedures
- Estimate time and cost for design transfer
- Coordinate with cross-site program management
- Synchronize with R&D, supply chain, and quality engineering
- Collaborate with manufacturing, production, OPEX, and finance
- Ensure design for manufacturability, assembly, and test
- Prepare plans to set up new production lines
- Execute plans to qualify new production lines
- Define and implement processes for resource availability
- Define and implement processes for high product quality
- Perform risk analysis and reporting
- Conduct risk review boards
- Define mitigation actions
- Implement mitigation actions
- Establish efficient communication for commitments and deadlines
- Establish efficient communication to resolve issues
- Define KPIs for design transfer metrics
- Monitor KPIs for design transfer metrics
Berufserfahrung
- 5 Jahre
Ausbildung
- Abgeschlossene Berufsausbildung
Sprachen
- Englisch – verhandlungssicher
- Deutsch – verhandlungssicher
Tools & Technologien
- ISO13485
- FDA21CFR820
- MDR
- GMP
Noch nicht perfekt?
- Thoratec Switzerland GmbHVollzeitnur vor OrtSeniorZürich
- Abbott Laboratories GmbH
Technical Writer – Medical Device(m/w/x)
Vollzeitnur vor OrtBerufserfahrenZürich - HITACHI ENERGY LTD
R&D Project Manager(m/w/x)
Vollzeitnur vor OrtBerufserfahrenZürich - HITACHI ENERGY LTD
Project Manager Secondary Engineering(m/w/x)
Vollzeitnur vor OrtBerufserfahrenZürich - SIEGFRIED DiNAMIQS AG
Head of Manufacturing and MSAT(m/w/x)
Vollzeitnur vor OrtManagementSchlieren
Manager NPI Engineering(m/w/x)
Driving design transfer for life-saving mechanical circulatory support devices, leading a team of up to 8 engineers at a global medical device manufacturer. 5+ years MedTech experience, 3+ years people leadership, and strong regulatory knowledge (ISO13485/FDA21CFR820/MDR/GMP) required. Team building focus, cross-site coordination.
Anforderungen
- Master’s degree in science or engineering
- Minimum 5 years’ experience in NPI, industrialization, or product creation
- Minimum 5 years in MedTech or pharma
- Strong knowledge of ISO13485/FDA21CFR820/MDR/GMP
- Minimum 3 years of people leadership
- Strong project management experience (cross-functional and multi-site)
- Excellent communication skills
- Fluent English (negotiation level)
- Further education in business, project management, or leadership
- Fluent German
- Experience in fast-paced, regulated environments
- Structured, analytical mindset and collaborative working style
- Openness to diverse cultures and ways of working
Aufgaben
- Build an NPI team of up to 8 engineers
- Lead an NPI team of up to 8 engineers
- Define design transfer work packages compliant with procedures
- Estimate time and cost for design transfer
- Coordinate with cross-site program management
- Synchronize with R&D, supply chain, and quality engineering
- Collaborate with manufacturing, production, OPEX, and finance
- Ensure design for manufacturability, assembly, and test
- Prepare plans to set up new production lines
- Execute plans to qualify new production lines
- Define and implement processes for resource availability
- Define and implement processes for high product quality
- Perform risk analysis and reporting
- Conduct risk review boards
- Define mitigation actions
- Implement mitigation actions
- Establish efficient communication for commitments and deadlines
- Establish efficient communication to resolve issues
- Define KPIs for design transfer metrics
- Monitor KPIs for design transfer metrics
Berufserfahrung
- 5 Jahre
Ausbildung
- Abgeschlossene Berufsausbildung
Sprachen
- Englisch – verhandlungssicher
- Deutsch – verhandlungssicher
Tools & Technologien
- ISO13485
- FDA21CFR820
- MDR
- GMP
Über das Unternehmen
Thoratec Switzerland GmbH
Branche
Healthcare
Beschreibung
The company is a global leader in life-saving medical technologies, supporting patients with advanced heart failure.
Noch nicht perfekt?
- Thoratec Switzerland GmbH
Senior Manufacturing Engineer(m/w/x)
Vollzeitnur vor OrtSeniorZürich - Abbott Laboratories GmbH
Technical Writer – Medical Device(m/w/x)
Vollzeitnur vor OrtBerufserfahrenZürich - HITACHI ENERGY LTD
R&D Project Manager(m/w/x)
Vollzeitnur vor OrtBerufserfahrenZürich - HITACHI ENERGY LTD
Project Manager Secondary Engineering(m/w/x)
Vollzeitnur vor OrtBerufserfahrenZürich - SIEGFRIED DiNAMIQS AG
Head of Manufacturing and MSAT(m/w/x)
Vollzeitnur vor OrtManagementSchlieren