Ingenieur Qualite jobs in United States
Ingénieure Qualité Pharma — Audit, CAPA & Libération
Capgemini
Supplier Quality Engineer - Welding & Supplier Development
TechnipFMC
Supplier Quality Engineer (Welding) - Supplier Excellence
TechnipFMC plc
Discover more opportunities than anywhere else. Find more jobs nowMethods & Tools Industrial Quality Engineer H/ F
ALSTOM Gruppe
Connect with headhunters to apply for similar jobsProduct Quality Engineer (F/M) Infrastructure & Quality Massy
Exotrail
Ingénieur Électricité Qualité H / F
B-Hive Engineering
Ingénieur Qualité Logiciel H / F
Ingeliance Technologies
Ingénieur Assurance Qualité Industrie Amélioration Continue
ARTHUS SOURCING
Ingénieur Électricité Qualité CFO/CFA – Projets industriels
B-Hive Engineering
Ingénieur Qualité Logiciel — Défense (Secret Habilitable)
Ingeliance Technologies
Ingénieur QA / Test Automation H/F
CELAD
Ingénieur Qualité Logiciel NPI — Santé Médicale
PowerToFly
Ingénieur Qualité Projets - Aéronautique & Industrialisation
LISI AEROSPACE
Ingénieur Support & Qualité – Programme Militaire
Sabena Technics
Ingénieur Support et Qualité Programme Militaire MCOC130J H / F
Sabena Technics
Ingénieur Qualité Logiciel – Conformité & Licences
THALES
Ingénieur/Soudeur IWT/IWE — Maîtrise procédés & qualité
GIS MIC (GLOBAL INTERNATIONAL SERVICES M
Ingénieur Soudage & Qualité ISO 9001 (IWE/IWT)
ARTIS
Quality Engineer (Medical Devices)
Job summary
A leading MedTech company in Valbonne is searching for a Quality Assurance Specialist. The role involves reviewing and validating compliance documentation, supporting project teams to meet quality standards, and collaborating with cross-functional teams. Required qualifications include extensive experience in Medical Devices, strong knowledge of ISO 13485 and IEC 60601 standards, and excellent English proficiency. Ideal candidates will have strong communication and leadership skills. This is a full-time position.
Responsibilities
- Review and validate all project/product documentation to ensure compliance with QMS and standards.
- Support and coach project teams to meet quality and regulatory requirements.
- Approve deliverables as QA representative.
- Collaborate with cross-functional teams to resolve quality or regulatory issues.
- Identify, assess, and manage risks related to safety, quality, and compliance.
- Analyse non-conformities and follow up CAPA actions.
Skills
Tools
Key Requirements
- Solid experience in Medical Devices (DM) or Electromedical Products
- Strong knowledge of ISO 13485 and IEC 60601 standards
- Good understanding of Quality Management Systems (QMS)
- Experience in or exposure to Quality Audits (internal / external)
- Ability to review and validate technical documentation for compliance
- Experience collaborating with R&D teams on design and product quality
- Excellent English level (American company all documentation and meetings in English)
- Strong communication coaching and leadership skills
Responsibilities
- Review and validate all project / product documentation to ensure compliance with QMS and standards (ISO 13485 / IEC 60601)
- Support and coach project teams to meet quality and regulatory requirements
- Approve deliverables as QA representative
- Collaborate with cross-functional teams to resolve quality or regulatory issues
- Identify assess and manage risks related to safety quality and compliance
- Analyse non-conformities define and follow up CAPA actions
Key Skills
APQP, Quality Assurance, Six Sigma, ISO 9001, PPAP, Minitab, Root cause Analysis, ISO 13485, Quality Systems, Quality Management, As9100, Manufacturing
Employment Type: Full Time
Experience: years
Vacancy: 1
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.