Senior Process Engineer – Medical Devices | Lean & Six Sigma

Jabil; Bettlach; Vor Ort; CHF 120.000 - 150.000; Vollzeit

Benefits dieser Stelle

Bonus system

Extra vacation days

Professional development

Zusammenfassung

Jabil Switzerland is seeking a Senior Process Engineer to lead process validation, optimization, and manufacturing support in a regulated medical device environment. You will drive data-driven improvements to reduce scrap and improve quality, applying Lean and Six Sigma methodologies and statistical analysis.

You will act as SME for manufacturing processes, collaborate with cross-functional teams, support IQ/OQ/PQ validation, and ensure compliance with GMP, GDP, and ISO 13485 across the site.

Qualifikationen

• Bachelor’s or Master’s degree in a technical field.
• 5+ years in medical device manufacturing or regulated industries.
• Strong expertise in manufacturing engineering and validation methodologies.
• Experience with GMP, GDP, and ISO 13485.
• Proficient in statistical analysis and problem solving.

Aufgaben

• Lead continuous improvement projects to boost productivity, quality, and efficiency.
• Analyze data to identify trends and optimize processes for scrap reduction.
• Act as SME for manufacturing processes to ensure quality and consistency.
• Develop and execute IQ/OQ/PQ validation protocols and docs.
• Provide day-to-day manufacturing support and implement corrective actions.
• Collaborate with cross-functional teams to improve performance and reliability.
• Support audits and ensure GMP/GDP compliance.
• Assist with new product introductions and process transfers.

Kenntnisse

Lean Manufacturing

Six Sigma

Data analysis

Process validation

Equipment qualification

GMP/GDP/ISO13485

Problem solving

ERP/MES exposure

Power BI

Ausbildung

Bachelor’s/Master’s in Mechanical/Manufacturing/Industrial Engineering

Tools

ERP/MES

Power BI

Jobbeschreibung

Jabil Switzerland is seeking a Senior Process Engineer to lead process validation, optimization, and manufacturing support in a regulated medical device environment. You will drive data-driven improvements to reduce scrap and improve quality, applying Lean and Six Sigma methodologies and statistical analysis.

You will act as SME for manufacturing processes, collaborate with cross-functional teams, support IQ/OQ/PQ validation, and ensure compliance with GMP, GDP, and ISO 13485 across the site.