Junior Supplier Quality Engineer

JR Italy; Verona; In loco; EUR 32.000 - 35.000; Tempo pieno

Descrizione del lavoro

An innovative firm is seeking a Junior Supplier Quality Engineer to join their Quality Operations team in Verona. This full-time role involves supporting supplier performance management, conducting audits, and utilizing statistical techniques to enhance processes. The ideal candidate will have a Master's degree in engineering and experience in the medical device sector, ensuring compliance with quality standards. With a friendly and inclusive work environment, this position offers competitive packages and opportunities for professional growth, making it an exciting opportunity for those passionate about quality engineering.

Servizi

Training and Development Opportunities

Competitive Packages

Social Events

Wellbeing Initiatives

Canteen

Pension Fund

Health Insurance

Competenze

• 2+ years of experience in quality or process engineering, preferably in medical devices.
• Familiarity with ISO 13485 and related regulations.

Mansioni

• Collaborate with supply chain to qualify and develop new suppliers.
• Conduct audits to evaluate supplier Quality Management Systems.

Conoscenze

Statistical Analysis

Root Cause Analysis

Problem Solving

Communication Skills

Formazione

Master’s Degree in Mechanical Engineering

Master’s Degree in Biomedical Engineering

Strumenti

Microsoft Office

Descrizione del lavoro

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Junior Supplier Quality Engineer, Verona

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Client:

Orthofix

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

519631947931477606433711

Job Views:

3

Posted:

26.04.2025

Expiry Date:

10.06.2025

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Job Description:

We offer an interesting opportunity to join our Quality Operations team, based in Bussolengo (VR), as Junior Supplier Quality Engineer, reporting to the Supplier Quality Engineer Supervisor.

In this position, you will support activities for supplier performance management, supplier audits, production flow validation, and monitoring. Specifically, you will handle product approval (PPAP, FAI), supplier performance monitoring (KPI, SCAR management), and planning and conducting supplier audits.

Responsibilities include:

1. Supplier Qualification: Collaborate with the International Supply Chain to select, qualify, and develop new suppliers, ensuring quality standards are met.
2. Supplier Audit: Conduct audits at supplier facilities to evaluate their Quality Management Systems, ensuring compliance with regulations such as ISO 13485 and FDA 21 CFR Part 820.
3. Supplier Monitoring: Use statistical techniques and Six Sigma methodologies to analyze processes, identify improvements, and implement corrective actions.
4. External Process Validation: Support suppliers in developing and validating manufacturing processes, including qualification of tools and testing methods.
5. Supplier non-conformities and SCAR management: Manage non-conformities, coordinate root cause investigations, and ensure corrective actions are implemented.

Qualifications:

• Master’s degree in mechanical, biomedical engineering, or similar preferred.
• At least 2 years of experience in quality, manufacturing, R&D, or process engineering, preferably in the medical device sector or other regulated industries.
• Excellent English skills, both written and spoken.
• Familiarity with ISO 13485, ISO 9001, and related regulations.
• Experience with statistical analysis, process validation (IQ, OQ, PQ), and quality control methodologies.
• Ability to conduct root cause analysis and lead investigations.
• Basic knowledge of technical design, process audits, measurement analysis (MSA, R&R), problem solving (8D, FMEA), and Control Plans.
• Proficiency in Microsoft Office.

Soft Skills:

• Excellent communication skills, effective in cross-functional teams.
• Problem-solving abilities.
• Ability to interact effectively with operational departments.

Benefits and Environment:

Friendly, innovative, and inclusive atmosphere with training and development opportunities, competitive packages, social events, wellbeing initiatives, canteen, pension fund, and health insurance.

Employment Details:

This is a full-time, permanent position with a salary range of €32,000 to €35,000, depending on experience and skills.