Supplier Quality Engineer II – Medical Devices, ISO/GMP

Integra LifeSciences Corporation

Le Locle

On-site

CHF 90,000 - 120,000

Full time

2 days ago
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Job summary

Integra LifeSciences Corporation in Le Locle, Switzerland, is seeking a skilled Supplier Quality Engineer to lead audits of contract manufacturers and suppliers. You will ensure compliance with GMP, ISO13485, and regulatory requirements while supporting QC, purchasing, and production teams.

The role requires a strong auditing background, knowledge of ISO standards, and fluency in French and English. Travel will be required as part of supplier oversight and continuous improvement initiatives.

Qualifications

  • Bachelor's degree in engineering, life science, or related technical field.
  • GMP/ISO regulated industry experience required.
  • Auditing background required; Lead Auditor ISO 13485:2016 preferred.
  • Fluent in French and English.
  • Willingness to travel.

Responsibilities

  • Lead supplier audits and ensure compliance with GMP and ISO standards.
  • Maintain Approved Supplier List and up-to-date supplier quality agreements.
  • Provide quality engineering support to QC, purchasing and production.
  • Report supplier performance metrics and drive CAPA.
  • Support internal and third-party audits/inspections.
  • Address supplier changes and validate outsourced processes.

Skills

Auditing
Supplier quality
Communication
Analytical problem solving
ERP/PLM
MS Office
Statistical methods
French & English
Willingness to travel

Education

Bachelor's degree in Engineering/Life Science
Education/experience equivalence

Tools

ERP systems
PLM systems
Microsoft Office

Job description

Integra LifeSciences Corporation in Le Locle, Switzerland, is seeking a skilled Supplier Quality Engineer to lead audits of contract manufacturers and suppliers. You will ensure compliance with GMP, ISO13485, and regulatory requirements while supporting QC, purchasing, and production teams.

The role requires a strong auditing background, knowledge of ISO standards, and fluency in French and English. Travel will be required as part of supplier oversight and continuous improvement initiatives.

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