Supplier Quality Engineer (m/f/d)

As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new day and our Mission to create ingenious solutions that ignite patient turnarounds. Our relentless commitment to patients and strong legacy of innovation in healthcare are the foundation of our future. If you're looking for a new chance, a new beginning, a new trajectory, LivaNova is where your talent can truly thrive. Join our talented team members worldwide to become a pioneer of tomorrow—because at LivaNova, we don’t just treat conditions — we aspire to alter the course of lives.

Supplier Quality Engineer (m/f/d)

Summary

The Supplier Quality Engineer (SQE) ensures that the supply chain companies continually develop their process in line with the design intent of the customer and verify their systems to ensure they are compliant with the end customer's needs. This includes on-going supply chain company verification. The SQE is responsible for delivering all aspects of the Supplier Quality Assurance function. The SQE collects root cause analysis and provides corrective feedback to prevent line stops due to supply issues. In addition the SQE manages the customer specific requirements and offers technical support to suppliers. The SQE is responsible for ensuring that the products produced meet quality standards required to minimize quality costs and maximize customer satisfaction whilst ensuring that procedures and processes are adhered to.

General Responsibilities

• Ensure that specifications cite critical characteristics and required process controls
• Provide technical development of the supplier throughout the product development process to assure launch readiness, including development and approval of supplier control plans (process validation requirements, sampling requirements)
• Establish incoming inspection plans for components with the supplier & LivaNova R&D department, assemblies and/or finished devices and quality department
• Assure the suppliers understanding of LivaNova products, their intended use, and regulatory requirements
• Ensure the proper risk controls are implemented at both supplier and LivaNova
• Ensure the measurement system at supplier & LivaNova are identical, and/or capable
• Monitor and analyze supplier data internally and externally gathered to identify trends and prevent potential problems
• Manage the Control and Manufacturing Process Change with the suppliers
• Initiate and manage Supplier Corrective Actions (SCAR) in partnership with Manufacturing/Process Engineering and Quality Engineering to ensure complete and effective root cause analysis and corrective action implementation is performed promptly
• Proactively to identify and help implement improvement to supplier quality and supplier quality tools and processes
• Collaborate with other members of the supply team to establish and maintain a meaningful supplier quality scorecard which is part of a bigger supplier scorecard that includes delivery, cost, partnership, etc.
• Manage the supplier quality audit process, which includes establishing requirements, setting priorities, determining audit frequency, and performing audits in a lead auditor role
• Travel Requirements 25 %

Skills and Experience

• Qualified Engineer or successfully completed University diploma with several years of industrial experience in manufacturing processes, or an equivalent education
• Knowledge of FDA, GMP, ISO 13485 and ISO 9001
• Ability to negotiate "win-win" situations with internal customers and external suppliers that meet LivaNova's business needs
• Ability to work in a highly matrixed and geographically diverse business environment
• Work with the Engineering (Design and Manufacturing Engineers) team to define process parameters and criteria to ensure supplier process capability is effective to meet product and process requirement
• Participate in cross-functional teams in the development of new products or changes related to current products in meeting customer requirements
• Advanced computer skills, including statistical/data analysis and report writing skills (Minitab knowledges appreciated)
• Good knowledge of Good Manufacturing Practices
• Fluent in English (written and spoken)
• Basic Knowledge of preferred techniques for continuous improvement such as Lean, Six-Sigma, Poka-Yoke (Error Proofing), Measurement System Analysis, and Process Failure Mode and Effects Analysis (PFMEA)
• Some years of experience in quality area
• Availability to travel to suppliers autonomously and able to integrate the different cultures
• Nice to have: ISO 9001 and/or 13485 auditor qualification

What we can offer you

In addition to providing you with a supportive, inclusive and collaborative environment where you will feel empowered to take ownership and drive meaningful change, we will reward you with the following:

• A dynamic role in an advanced Medical Device environment interfacing with all worldwide regulatory landscapes supporting your professional career growth
• Exposure to a State-of-the-Art medical device development process, in close co-operation with international clinicians
• Competitive base salary
• Variable short-term & long-term incentives

• Recognition: through our STARS Program, we recognize and celebrate our colleagues’ contributions and achievements

If you like the sound of the above and feel energized by the idea of joining a great brand at a moment of exciting expansion, please apply now. We look forward to hearing from you!

Welcome to impact. Welcome to innovation. Welcome to your new life.