Junior Supplier Quality Engineer

Social network you want to login/join with: Junior Supplier Quality Engineer, Bussolengo Client: Orthofix Location: Bussolengo Job Category: Other EU work permit required: Yes Job Reference: 630679457804949913633710 Job Views: 4 Posted: 11.03.2025 Expiry Date: 25.04.2025 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 be in charge of support activities for supplier performance management, supplier audit, production flow validation, and monitoring. Specifically, you will deal with the approval of products supplied (PPAP, FAI), monitoring and management of suppliers’ performances (KPI, SCAR management), and supplier audits planning and management. What will your contribution be? Supplier Qualification: Collaborate with International Supply Chain to select, qualify, and develop new suppliers, ensuring they meet the required quality standards. Supplier Audit: Conduct audits at supplier facilities to evaluate their Quality Management Systems, ensuring compliance with applicable regulations such as ISO 13485 and FDA 21 CFR Part 820. Supplier Monitoring: Use statistical techniques and Six Sigma methodologies to analyze supplier processes, identify areas for improvement, and implement corrective and preventive actions. External Process Validation: Support suppliers in the development and validation of manufacturing processes, including the qualification of tools and testing methods, to ensure the quality of supplied components. Supplier Non-Conformities and SCAR Management: Manage supplier-related non-conformities, coordinate root cause investigations, and ensure the implementation of effective corrective actions. What are we looking for? Master’s degree in mechanical or biomedical engineering or similar is preferred. At least 2 years of experience in quality, manufacturing, research and development, or process engineering roles, preferably in the medical device sector or other highly regulated industries. Excellent English written and spoken required. Familiarity with applicable regulations and standards, such as ISO 13485 and ISO 9001. Experience with statistical analysis techniques, process validation (IQ, OQ, PQ), and quality control methodologies. Ability to conduct root cause analysis and lead non-conformity investigations. Basic knowledge of technical design, process audit, measurement analysis (MSA, R&R), problem solving (8D, FMEA), Control Plan. Good knowledge of Microsoft Office. What soft skills are we looking for? Excellent written and oral communication abilities, with experience working effectively in cross-functional teams. Problem solving. Ability to interact with operational departments. What will you find? Friendly, warm, and innovative atmosphere. Healthy, inspiring, and international and inclusive work environment. Training and development opportunities. Competitive reward packages. Social and company events. Canteen. Benefits (Pension Fund - Health Insurance). What we offer? This is a full-time job. The contract is a permanent contract. Salary package range: 32,000/35,000 euro Please note that this is a range; the complete salary package will be defined based on the seniority/skills of the person. J-18808-Ljbffr

Location: bussolengo, IT

Posted Date: 3/17/2025