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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!
Our commitment to Diversity & Inclusion:
LivaNova values equality and celebrates diversity. We are committed to ensuring that our recruitment process is fair, transparent and free from unlawful discrimination.
Our selection process is driven by the key demands/requirements for the role rather than bias or discrimination on the basis of a candidate’s sex, gender identity, age, marital status, veteran status, non-job-related disability/handicap or medical condition, family status, sexual orientation, religion, color, ethnicity, race or any other legally protected classification.
Notice to third party agencies:
Please note that we do not accept unsolicited resumes from recruiters or employment agencies. In the absence of a signed Recruitment Services Agreement, we will not consider, or agree to, payment of any referral compensation or recruiter fee. In the event that a recruiter or agency submits a resume or candidate without a previously signed agreement, we explicitly reserve the right to pursue and hire those candidate(s) without any financial obligation to the recruiter or agency.
Beware of Job Scams:
Please beware of potentially fraudulent job postings or suspicious recruiting activity by persons posing as LivaNova recruiters or employees. The scammers may attempt to solicit confidential, personal information, such as a social security number, or your financial information. LivaNova will never ask for fees prior/during/after the application process, nor will we ask for banking details or personal financial information in return for the assurance of employment. If you are concerned that an offer of employment might be a scam or that the recruiter is not legitimate, please verify by searching for “See Open Jobs” on https://www.livanova.com/en-us/careers, and check that all recruitment emails come from an @livanova.com email address.
Top Skills
What We Do
LivaNova PLC is a global medical technology company built on nearly five decades of experience and a relentless commitment to improve the lives of patients around the world. Our advanced technologies and breakthrough treatments provide meaningful solutions for the benefit of patients, healthcare professionals and healthcare systems.
At LivaNova, we understand the importance of bringing both clinical and economic value to our customers. We are a strong, market-leading medical technology and services company, offering a diverse product portfolio and global reach. LivaNova is listed on the NASDAQ stock exchange under the ticker symbol “LIVN.”
LivaNova has approximately 3,000 employees worldwide. We are headquartered in London (UK) and maintain a presence in more than 100 countries. LivaNova operates as two businesses:
We have a strong legacy as leaders in neuromodulation and cardiovascular solutions, providing products and therapies in distinct therapeutic areas to treat the head and heart. These include:
• Difficult-to-Treat Depression
• Drug-Resistant Epilepsy
• Obstructive Sleep Apnea
• Advanced Circulatory Support
• Heart Failure
• Cardiopulmonary
At LivaNova, we serve health and improve lives. Day by day. Life by life.