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Process Engineer(m/w/x)
Root cause analysis and CAPA management for large-scale electronics manufacturing services. Proven experience with non-conformance investigations and regulatory quality standards required. Reasonable accommodation for disability provided.
Requirements
- Degree in Mechanical, Manufacturing, Industrial Engineering, or related
- Experience in manufacturing, process, or quality engineering
- Strong knowledge of NC/CAPA processes
- Familiarity with regulatory and quality standards
- Excellent problem-solving, analytical, and documentation skills
- Proficiency in process improvement tools
- Strong communication and teamwork skills
- Proven experience in project leadership
- Fluency in English and ideally German
- Attention to detail and organizational skills
- Ability to manage multiple priorities
- Continuous improvement mindset and proactive approach
- Commitment to quality and compliance
Tasks
- Support and improve manufacturing processes
- Ensure product quality and operational efficiency
- Lead investigations for non-conformances, CAPAs, and audit observations
- Document product bounding and disposition
- Perform root cause analysis for quality issues
- Define corrective and preventive actions
- Lead cross-functional investigation teams
- Ensure timely implementation of corrections and CAPAs
- Prepare and maintain documentation for process improvements
- Serve as subject matter expert for audit deviations
- Analyze processes to optimize quality, cost, and throughput
- Revise work instructions and standard operating procedures
- Maintain compliance with ISO, FDA, and GMP requirements
- Collaborate with Quality, R&D, Production, and Supply Chain teams
- Provide technical support and training to production personnel
- Contribute to manufacturing best practices and continuous improvement
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- NC/CAPA
- ISO 13485
- FDA 21 CFR Part 820
- GMP
- Lean
- Six Sigma
Benefits
Other Benefits
- Reasonable accommodation for disability
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Process Engineer(m/w/x)
Root cause analysis and CAPA management for large-scale electronics manufacturing services. Proven experience with non-conformance investigations and regulatory quality standards required. Reasonable accommodation for disability provided.
Requirements
- Degree in Mechanical, Manufacturing, Industrial Engineering, or related
- Experience in manufacturing, process, or quality engineering
- Strong knowledge of NC/CAPA processes
- Familiarity with regulatory and quality standards
- Excellent problem-solving, analytical, and documentation skills
- Proficiency in process improvement tools
- Strong communication and teamwork skills
- Proven experience in project leadership
- Fluency in English and ideally German
- Attention to detail and organizational skills
- Ability to manage multiple priorities
- Continuous improvement mindset and proactive approach
- Commitment to quality and compliance
Tasks
- Support and improve manufacturing processes
- Ensure product quality and operational efficiency
- Lead investigations for non-conformances, CAPAs, and audit observations
- Document product bounding and disposition
- Perform root cause analysis for quality issues
- Define corrective and preventive actions
- Lead cross-functional investigation teams
- Ensure timely implementation of corrections and CAPAs
- Prepare and maintain documentation for process improvements
- Serve as subject matter expert for audit deviations
- Analyze processes to optimize quality, cost, and throughput
- Revise work instructions and standard operating procedures
- Maintain compliance with ISO, FDA, and GMP requirements
- Collaborate with Quality, R&D, Production, and Supply Chain teams
- Provide technical support and training to production personnel
- Contribute to manufacturing best practices and continuous improvement
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- NC/CAPA
- ISO 13485
- FDA 21 CFR Part 820
- GMP
- Lean
- Six Sigma
Benefits
Other Benefits
- Reasonable accommodation for disability
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Jabil Switzerland Manufacturing GmbH
Industry
Manufacturing
Description
Das Unternehmen ist der weltweit größte Hersteller von Healthcare-Design und Herstellungsdienstleistungen und verbessert die Gesundheit der Menschen.
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