Senior Medical Device Process Engineer — Lean Six Sigma

Jabil

Solothurn

Vor Ort

CHF 80.000 - 110.000

Vollzeit

14 Tage+

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Benefits dieser Stelle

Bonus system
Extra vacation days
Responsible and varied job

Zusammenfassung

Jabil in Solothurn, Switzerland, seeks a Senior Process Engineer responsible for process validation and manufacturing support within a regulated medical device manufacturing environment. The role involves process optimization, data analysis, and ensuring compliance with GMP, GDP, and ISO 13485 standards.

This position requires a Bachelor's or Master's degree in Engineering and at least 5 years of experience in medical device manufacturing. Join us to make a significant impact while enjoying progressive employment conditions and various benefits.

Qualifikationen

  • Minimum 5+ years of experience in medical device manufacturing or other highly regulated industries.
  • Lean Six Sigma Green Belt certification desired.
  • Strong experience in manufacturing engineering, process optimization, and validation methodologies.
  • Knowledge of statistical analysis tools and structured problem-solving methodologies.

Aufgaben

  • Lead continuous improvement initiatives focused on productivity and quality.
  • Analyze manufacturing data to identify trends and optimize processes.
  • Develop and execute process validation activities including IQ/OQ/PQ protocols.
  • Collaborate with cross-functional teams to improve manufacturing performance.

Kenntnisse

Process optimization
Lean Manufacturing
Six Sigma methodologies
Data analysis
Statistical tools
Technical support
Regulatory compliance
Analytical skills

Ausbildung

Bachelor’s or Master’s degree in Mechanical Engineering

Tools

ERP/MES systems
Power BI

Jobbeschreibung

Jabil in Solothurn, Switzerland, seeks a Senior Process Engineer responsible for process validation and manufacturing support within a regulated medical device manufacturing environment. The role involves process optimization, data analysis, and ensuring compliance with GMP, GDP, and ISO 13485 standards.

This position requires a Bachelor's or Master's degree in Engineering and at least 5 years of experience in medical device manufacturing. Join us to make a significant impact while enjoying progressive employment conditions and various benefits.

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