Dein persönlicher KI-Karriere-Agent
Quality Engineer(m/w/x)
Creating quality control documents for medical devices, including First Article Inspection instructions. ISO 13485 and 21CFR820 experience required. Bonus system, extra vacation days, and long-term perspective.
Anforderungen
- Bachelor’s degree or equivalent education/experience
- Manufacturing, quality, or engineering experience required
- ISO 13485 and 21CFR820 medical device industry experience
- CNC and surface treatment experience is a plus
- Production and quality system MES, SAP, ETQ, Babtec experience is a plus
- Strong analytical, problem-solving, data-interpretation skills
- Familiarity with statistical analysis tools/methods (SPC, capability studies)
- Cross-functional work and effective communication skills
- High attention to detail and quality commitment
- Ability to follow procedures and comply with safety/security
- Fluent English and German
Aufgaben
- Collaborate with production and engineering teams
- Ensure products meet quality and regulatory requirements
- Create quality control documents
- Recommend quality control tools and methods
- Prepare First Article Inspection instructions
- Assess nonconforming products
- Recommend product disposition
- Support quality issues resolution
- Participate in nonconformities investigations
- Participate in CAPA investigations
- Support product disposition
- Implement quality improvements
- Monitor CAPA effectiveness
- Lead product and process improvement efforts
- Use CAPA and Kaizen methodology
- Act as SME for projects
- Support new equipment introduction
- Support new product introduction
- Support product and process improvements
- Prepare for internal and external audits
- Conduct Gemba walks
- Implement remediation actions
- Support manufacturing process risk assessment
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – fließend
- Deutsch – fließend
Tools & Technologien
- ISO 13485
- 21CFR820
- MES
- SAP
- ETQ
- Babtec
- SPC
- capability studies
Benefits
Boni & Prämien
- Bonus system
Mehr Urlaubstage
- Extra vacation days
Sicherer Arbeitsplatz
- Long-term perspective
Sinnstiftende Arbeit
- High level of personal responsibility
- Independent work
Lockere Unternehmenskultur
- Safe space for creative thinking
Weiterbildungsangebote
- Learning at the workplace
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Quality Engineer(m/w/x)
Creating quality control documents for medical devices, including First Article Inspection instructions. ISO 13485 and 21CFR820 experience required. Bonus system, extra vacation days, and long-term perspective.
Anforderungen
- Bachelor’s degree or equivalent education/experience
- Manufacturing, quality, or engineering experience required
- ISO 13485 and 21CFR820 medical device industry experience
- CNC and surface treatment experience is a plus
- Production and quality system MES, SAP, ETQ, Babtec experience is a plus
- Strong analytical, problem-solving, data-interpretation skills
- Familiarity with statistical analysis tools/methods (SPC, capability studies)
- Cross-functional work and effective communication skills
- High attention to detail and quality commitment
- Ability to follow procedures and comply with safety/security
- Fluent English and German
Aufgaben
- Collaborate with production and engineering teams
- Ensure products meet quality and regulatory requirements
- Create quality control documents
- Recommend quality control tools and methods
- Prepare First Article Inspection instructions
- Assess nonconforming products
- Recommend product disposition
- Support quality issues resolution
- Participate in nonconformities investigations
- Participate in CAPA investigations
- Support product disposition
- Implement quality improvements
- Monitor CAPA effectiveness
- Lead product and process improvement efforts
- Use CAPA and Kaizen methodology
- Act as SME for projects
- Support new equipment introduction
- Support new product introduction
- Support product and process improvements
- Prepare for internal and external audits
- Conduct Gemba walks
- Implement remediation actions
- Support manufacturing process risk assessment
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – fließend
- Deutsch – fließend
Tools & Technologien
- ISO 13485
- 21CFR820
- MES
- SAP
- ETQ
- Babtec
- SPC
- capability studies
Benefits
Boni & Prämien
- Bonus system
Mehr Urlaubstage
- Extra vacation days
Sicherer Arbeitsplatz
- Long-term perspective
Sinnstiftende Arbeit
- High level of personal responsibility
- Independent work
Lockere Unternehmenskultur
- Safe space for creative thinking
Weiterbildungsangebote
- Learning at the workplace
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
Jabil Switzerland Manufacturing GmbH
Branche
Manufacturing
Beschreibung
Das Unternehmen ist der weltweit größte Hersteller von Healthcare-Design und Herstellungsdienstleistungen und verbessert die Gesundheit der Menschen.
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