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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.
Requirements
- 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
Tasks
- 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
Work Experience
- 4 - 7 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- ISO 13485
- ISO 14971
- FDA
- Lean Manufacturing
- Six Sigma
- MS Office
- Word
- Excel
- Outlook
Benefits
Flexible Working
- Flexible work arrangements
Family Support
- Work-life balance
Mentorship & Coaching
- Well-being and development investment
Bonuses & Incentives
- Rewards and recognition opportunities
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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.
Requirements
- 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
Tasks
- 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
Work Experience
- 4 - 7 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- ISO 13485
- ISO 14971
- FDA
- Lean Manufacturing
- Six Sigma
- MS Office
- Word
- Excel
- Outlook
Benefits
Flexible Working
- Flexible work arrangements
Family Support
- Work-life balance
Mentorship & Coaching
- Well-being and development investment
Bonuses & Incentives
- Rewards and recognition opportunities
About the Company
Becton, Dickinson and Company
Industry
Healthcare
Description
The company is a global leader in medical technology, advancing health through innovation in medical discovery, diagnostics, and care delivery.
Not a perfect match?
- Becton, Dickinson and Company
Quality Engineer – Medical Devices(m/w/x)
Full-timeOn-siteExperiencedVilters-Wangsfrom CHF 145,775 / year - Hamilton Bonaduz AG
Electrical Engineer(m/w/x)
Full-timeOn-siteExperiencedEms - Hamilton Bonaduz AG
Projektleitung für Produktentwicklung(m/w/x)
Full-timeOn-siteSeniorEms - Hamilton Bonaduz AG
Quality Manager(m/w/x)
Full-timeOn-siteJuniorEms - Körber Pharma Packaging AG
Automation Engineer Assembly / Labelling(m/w/x)
Full-timeOn-siteExperiencedGrabs