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Manufacturing Engineer(m/w/x)
Design and implementation of medical device manufacturing processes for specification remediation projects. Industrial experience in FDA or ISO regulated environments required. Flexible work arrangements, 30 days vacation.
Anforderungen
- Degree in Mechanical, Biomedical, or related engineering
- Biomedical Engineering or Bioengineering Master’s preferred
- Industrial experience in medical device environments
- Experience designing, manufacturing, or prototyping medical devices
- Experience in regulated environments (ISO, FDA)
- Knowledge of Lean Manufacturing and Six Sigma
- Self-motivated, team-oriented, and solution-focused
- Fluent in English, written and spoken
- Fluency in German is a strong plus
- Very good organization and planning skills
- Ability to lead projects with teams
- Effective communication skills
- Good skills in MS Office
Aufgaben
- Design and implement new medical device products
- Develop efficient manufacturing processes and test methods
- Execute design changes for specification remediation projects
- Conduct engineering studies for process improvements
- Identify and implement cost-saving opportunities
- Lead and coordinate validation and improvement projects
- Collaborate with cross-functional teams on continuous improvement
- Comply with safety regulations and promote best practices
- Specify and revise manufacturing documentation for components
- Lead OpEx, Lean, and Six Sigma initiatives
- Provide technical support to R&D, QE, QA, and production
- Perform Design of Experiments and process capability analyses
- Conduct root cause analyses using 5 Whys and Ishikawa
- Analyze data and interpret results using Minitab
- Write technical reports and statistical summaries
- Support production lines and transfer new products
- Execute and document DVVs and process validations
- Support Test Method Validations
- Apply basic tooling, design, and drafting knowledge
- Monitor processes and collect performance data
- Document activities according to regulatory and internal standards
Berufserfahrung
Ausbildung
Sprachen
Tools & Technologien
Benefits
Flexibles Arbeiten
- •Flexible work arrangements
Familienfreundlichkeit
- •Work-life balance
Mentoring & Coaching
- •Well-being and development investment
Boni & Prämien
- •Rewards and recognition opportunities
- Becton, Dickinson and CompanyVollzeitnur vor OrtBerufserfahrenab CHF 145.775 / JahrVilters-Wangs
- Körber Pharma Packaging AG
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Manufacturing Engineer(m/w/x)
Design and implementation of medical device manufacturing processes for specification remediation projects. Industrial experience in FDA or ISO regulated environments required. Flexible work arrangements, 30 days vacation.
Anforderungen
- Degree in Mechanical, Biomedical, or related engineering
- Biomedical Engineering or Bioengineering Master’s preferred
- Industrial experience in medical device environments
- Experience designing, manufacturing, or prototyping medical devices
- Experience in regulated environments (ISO, FDA)
- Knowledge of Lean Manufacturing and Six Sigma
- Self-motivated, team-oriented, and solution-focused
- Fluent in English, written and spoken
- Fluency in German is a strong plus
- Very good organization and planning skills
- Ability to lead projects with teams
- Effective communication skills
- Good skills in MS Office
Aufgaben
- Design and implement new medical device products
- Develop efficient manufacturing processes and test methods
- Execute design changes for specification remediation projects
- Conduct engineering studies for process improvements
- Identify and implement cost-saving opportunities
- Lead and coordinate validation and improvement projects
- Collaborate with cross-functional teams on continuous improvement
- Comply with safety regulations and promote best practices
- Specify and revise manufacturing documentation for components
- Lead OpEx, Lean, and Six Sigma initiatives
- Provide technical support to R&D, QE, QA, and production
- Perform Design of Experiments and process capability analyses
- Conduct root cause analyses using 5 Whys and Ishikawa
- Analyze data and interpret results using Minitab
- Write technical reports and statistical summaries
- Support production lines and transfer new products
- Execute and document DVVs and process validations
- Support Test Method Validations
- Apply basic tooling, design, and drafting knowledge
- Monitor processes and collect performance data
- Document activities according to regulatory and internal standards
Berufserfahrung
Ausbildung
Sprachen
Tools & Technologien
Benefits
Flexibles Arbeiten
- •Flexible work arrangements
Familienfreundlichkeit
- •Work-life balance
Mentoring & Coaching
- •Well-being and development investment
Boni & Prämien
- •Rewards and recognition opportunities
Über das Unternehmen
Becton, Dickinson and Company
Branche
Healthcare
Beschreibung
The company is a global leader in medical technology, advancing health through innovation in medical discovery, diagnostics, and care delivery.
- Becton, Dickinson and Company
Quality Engineer – Medical Devices(m/w/x)
Vollzeitnur vor OrtBerufserfahrenab CHF 145.775 / JahrVilters-Wangs - Körber Pharma Packaging AG
Quality Process Engineer(m/w/x)
Vollzeitnur vor OrtBerufserfahrenGrabs - Hamilton Bonaduz AG
Praktikum im Process Engineering(m/w/x)
VollzeitPraktikumnur vor OrtEms - Hamilton Bonaduz AG
Electrical Engineer(m/w/x)
Vollzeitnur vor OrtBerufserfahrenEms - Straub Medical AG
Polymechaniker CNC Langdrehen(m/w/x)
Vollzeitnur vor OrtBerufserfahrenab CHF 91.500 / JahrVilters-Wangs