Junior Medical Device Manufacturing Engineer - Lean Process

Jobtailor; Aarau; Vor Ort; CHF 110.000 - 160.000; Vollzeit

Zusammenfassung

Smith & Nephew Manufacturing AG is seeking a committed professional to lead design and manufacturing transfers and drive internal projects within defined time, quality, and cost boundaries.

You will act as the SME for manufacturing processes and develop compliant solutions for advanced medical devices, including risk assessments and process characterization. Strong documentation skills and MS Office proficiency are essential.

Qualifikationen

• Engineering degree or HF/Technician grade with limited or no relevant work experience.
• Knowledge of quality control, risk mitigation and statistical process control techniques.
• Analytical skills, problem solving methods and ability to develop long term solutions.
• Knowledge of Lean management tools.
• Proficient in Word, Excel, and PowerPoint.
• Ability to communicate and write documentation/reports in English.

Aufgaben

• Lead design/manufacturing transfers, internal manufacturing projects, and manufacturing changes within defined time, quality and cost boundaries.
• Plan and control project execution, including scheduling, budgeting, progress tracking, and governance reporting.
• Act as SME for manufacturing processes, developing and implementing compliant solutions for advanced medical devices.
• Perform and lead process risk assessments and process characterization or capability studies.
• Provide technical support for changes and quality issues related to manufacturing, quality and suppliers.
• Create and maintain compliant technical documentation (DHF, DMRs, MBOMs in Windchill PLM).

Kenntnisse

Analytical skills

Problem solving

Communication

Documentation writing

Ausbildung

Engineering degree

HF

Technician grade

Tools

Windchill PLM

MS Office

Jobbeschreibung

Smith & Nephew Manufacturing AG is seeking a committed professional to lead design and manufacturing transfers and drive internal projects within defined time, quality, and cost boundaries.

You will act as the SME for manufacturing processes and develop compliant solutions for advanced medical devices, including risk assessments and process characterization. Strong documentation skills and MS Office proficiency are essential.