Senior Supplier Quality Engineer

Abbott; Zürich; Vor Ort; CHF 80’000 - 100’000; Vollzeit

Zusammenfassung

A leading company in the medical devices sector is seeking a Senior Supplier Quality Engineer in Zurich. The role involves ensuring supplier compliance, conducting audits, and collaborating with cross-functional teams to enhance quality. Candidates should possess a bachelor's degree in relevant fields, 5+ years of experience, and fluency in German and English.

Leistungen

Career development opportunities

Competitive compensation and benefits

Workplace in the heart of Zurich

Qualifikationen

• 5+ years of experience in supplier quality engineering or similar role.
• Proficiency in written and spoken German and English.
• Certification as ISO and/or ISO Auditor.
• Certification in quality management (e.g., Six Sigma) is a plus.

Aufgaben

• Develop and maintain supplier quality assurance processes.
• Conduct supplier audits and assessments.
• Lead root cause analysis and problem-solving for quality issues.

Kenntnisse

Problem-solving

Root cause analysis

Quality assurance principles

Interpersonal communication

Ausbildung

Bachelor's degree in engineering, quality management, or a related field

Tools

Quality tools and software

Jobbeschreibung

We are seeking a detail-oriented and experienced Senior Supplier Quality Engineer to join our team.

Main Responsibilities :

1. Supplier Quality Assurance : Develop and maintain supplier quality assurance processes and procedures. Work closely with suppliers to resolve quality issues, implement corrective actions, and provide technical support and guidance on quality-related matters. Review and approve supplier quality documentation. Monitor and manage Supplier Change Requests in cooperation with a cross-functional team. Evaluate and qualify new suppliers based on their ability to meet quality and performance standards. Ensure Supplier Quality Agreements are established. Conduct initial assessments and supplier audits to ensure suppliers can deliver high-quality products and materials in accordance with medical device requirements.
2. Supplier Audits and Assessments : Conduct supplier audits and assessments to ensure compliance with quality standards. Maintain and manage the approved supplier list. Conduct regular reviews and re-qualifications of existing suppliers to ensure ongoing compliance with quality standards and current certification. Continuously monitor and evaluate supplier performance using key performance indicators (KPIs). Identify trends and areas for improvement, and work with suppliers to implement corrective actions and enhance overall performance. Lead Continuous Improvement Initiatives based on supplier performance. Prepare and present quality reports and metrics to management.
3. Cross-Functional Collaboration : Work closely with cross-functional teams, including engineering, procurement, and manufacturing, to address quality-related issues and supplier change requests.
4. Root Cause Analysis : Lead root cause analysis and problem-solving activities for supplier-related quality issues. Lead the investigation and resolution of supplier-related non-conformances. Document and track NCMRs, ensuring timely and effective corrective actions. Drive the CAPA process to identify root causes of quality issues, implement corrective actions, and verify their effectiveness. Develop preventive measures to avoid recurrence.

Qualifications :

• Bachelor's degree in engineering, quality management, or a related field.
• Experience in Medical Devices or similar industry.
• Excellent problem-solving skills and experience with root cause analysis methodologies.
• Proficient in using quality tools and software.
• Proficiency in both written and spoken German and English.
• Minimum of 5 years of experience in supplier quality engineering or a similar role.
• Strong knowledge of quality assurance principles, methodologies, and tools.
• Experience with supplier audits and assessments.
• Strong communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Certification as ISO and/or ISO Auditor (or comparable qualification).
• Certification in quality management (e.g., Six Sigma) is a plus.

Working at Abbott

At Abbott, you can do work that matters and help people live healthier and fuller lives, grow your career, and learn. You will have access to:

• Career development with an international company where you can grow
• A workplace in a Fortune 500 company and the world’s leading manufacturer of medical devices
• A challenging position in a crisis-independent industry
• The opportunity to be part of a dynamic, highly educated, and motivated team
• A multi-national environment fostering talent development
• Competitive compensation and benefits
• A workplace in the heart of Zurich

We are looking for a highly motivated person who would like to be part of our passionate team with broad responsibilities. Do you have what it takes? Then send us your application including motivation letter, curriculum vitae, letter of recommendation, and diplomas today. We look forward to meeting you in Zurich!

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