Senior Manufacturing Engineer

Jabil; Bettlach; Vor Ort; CHF 120.000 - 160.000; Vollzeit

Benefits dieser Stelle

Bonus system

Extra vacation days

Zusammenfassung

Jabil, a global engineering and manufacturing solutions leader, seeks an experienced Manufacturing Process Engineer for its medical device operations in Switzerland. You will lead continuous improvement, analyze data, and drive process validation, while collaborating across production, quality, maintenance, and engineering to ensure product quality and regulatory compliance.

With 5+ years in regulated manufacturing, you will influence efficiency, scrap reduction, and process reliability, and

Qualifikationen

• Bachelor’s or Master’s degree in Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, or a related technical field.
• Lean Six Sigma Green Belt certification desired.
• Strong experience in manufacturing engineering, process optimization, and validation methodologies.

Aufgaben

• Lead continuous improvement initiatives focused on productivity, quality, cost reduction, and operational efficiency within a medical device manufacturing environment.
• Analyze manufacturing data to identify trends and root causes, and perform process optimization for scrap reduction and efficiency improvement using Lean Manufacturing, Six Sigma methodologies, statistical analysis, and process capability studies.
• Act as SME for assigned manufacturing processes, optimizing operations to ensure product quality, process consistency, and efficiency.
• Develop and execute process validation activities including IQ/OQ/PQ protocols and validation documentation.
• Provide day-to-day manufacturing and business support to production operations and cross-functional teams, including troubleshooting and corrective actions.
• Collaborate with production, quality, maintenance, and engineering teams to improve performance and reliability.
• Support new product introductions, process transfers, equipment qualifications, risk assessments, and FMEA activities, while supporting internal and external audits and ensuring GMP/GDP/ISO13485 compliance.

Kenntnisse

Lean Six Sigma

Analytical thinking

Project management

Statistical analysis

Ausbildung

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

Tools

Power BI

ERP/MES systems

Jobbeschreibung

At Jabil (NYSE: JBL), we are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, supply chain, and manufacturing solutions. With 60 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe.

Responsibilities

• Lead continuous improvement initiatives focused on productivity, quality, cost reduction, and operational efficiency within a medical device manufacturing environment.
• Analyze manufacturing data to identify trends and root causes, and perform process optimization for scrap reduction and efficiency improvement using Lean Manufacturing, Six Sigma methodologies, statistical analysis, and process capability studies.
• Act as Subject Matter Expert (SME) for assigned manufacturing processes, optimizing manufacturing operations to ensure product quality, process consistency, and operational efficiency.
• Develop and execute process validation activities including IQ/OQ/PQ protocols and validation documentation.
• Provide day-to-day manufacturing and business support to production operations and cross-functional teams, including troubleshooting and implementation of corrective actions for manufacturing and process-related issues.
• Collaborate with production, quality, maintenance, and engineering teams to improve manufacturing performance and process reliability.
• Support new product introductions, process transfers, equipment qualifications, risk assessments, and FMEA activities, while also supporting internal and external audits and ensuring compliance with regulatory and quality standards.
• Ensure manufacturing processes comply with GMP (Good Manufacturing Practice) and GDP (Good Documentation Practice) requirements

Background

• Bachelor’s or Master’s degree in Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, or a related technical field.
• 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.
• Hands-on experience with process validation, equipment qualification, and manufacturing process controls.
• Strong understanding of GMP, GDP, ISO 13485, and regulated manufacturing environments.
• Knowledge of statistical analysis tools and structured problem-solving methodologies.
• Excellent analytical, communication, and project management skills.
• Experience with ERP/MES systems and manufacturing data reporting tools is an advantage.
• Power BI skills and experience with data visualization/reporting tools are a plus.

Reporting

You are reporting to Process Engineering Supervisor II

Offer

• A responsible and varied job in a global company with a strong local presence
• Progressive employment conditions with long-term perspective
• A high level of personal responsibility and independent work
• A safe space for creative thinking and learning at the workplace
• Bonus system, extra vacation days and many other benefits
• Find out more about JABIL Switzerland.

Jabil, including its subsidiaries, is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, age, disability, genetic information, veteran status, or any other characteristic protected by law.

Accessibility Accommodation

Accessibility Accommodation If you are a qualified individual with a disability, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access Jabil.com/Careers site as a result of your disability. You can request a reasonable accommodation by sending an e‑mail to [e-mail] with the nature of your request and contact information. Please do not direct any other general employment related questions to this e‑mail. Please note that only those inquiries concerning a request for reasonable accommodation will be responded to.

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