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Supplier Quality Engineer - Medical Devices

JR Italy

Brescia

In loco

EUR 35.000 - 55.000

Tempo pieno

9 giorni fa

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Descrizione del lavoro

An established industry player in medical device manufacturing is looking for a Supplier Quality Engineer to ensure the highest quality standards in supplier management. In this pivotal role, you will conduct audits, support the Quality Control department, and assist in launching new product lines with external suppliers. This position offers a unique opportunity to contribute to the company's quality system and work closely with a dedicated team. If you have a passion for quality management and a background in technical disciplines, this role is perfect for you.

Competenze

  • 3+ years of experience in quality management and supplier audits.
  • Certification as an Auditor according to ISO standards is required.

Mansioni

  • Conduct supplier audits and internal audits within the group.
  • Support the Quality Control department in supplier-related issues.

Conoscenze

Quality Management
Supplier Audits
Internal Audits
Problem Solving
English Language

Formazione

Diploma or Degree in Technical Disciplines

Descrizione del lavoro

Job Opportunity: Supplier Quality Engineer in Brescia, Italy

We are seeking a Supplier Quality Engineer for a leading company in the design and manufacturing of medical devices.

Main Responsibilities:
  1. Conduct supplier audits;
  2. Perform internal audits within the group;
  3. Support the Quality Control department in addressing supplier-related issues;
  4. Assist in the launch and qualification of new product lines and customized components with external suppliers;
  5. Support the Quality Assurance Manager in managing and maintaining the company's quality system.
Qualifications:
  • Diploma or Degree in technical disciplines;
  • Certification as an Auditor according to ISO 9001, ISO 13485, ISO 45000, ISO 14001;
  • At least 3 years of experience in quality management;
  • Knowledge of the English language;
  • (Preferred) Certification as an internal auditor according to VDA 6.3 or equivalent.
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