Supplier Quality Engineer

Supplier Quality Engineer

Siemens Healthineers has an opening for a Supplier Quality Engineer at our In-Vitro Diagnostic (IVD) instrumentation / reagent manufacturing site in Llanberis, Gwynedd, North Wales. The Supplier Quality team works cross-functionally with engineering, production, and procurement with responsibilities focused on maintaining a high level of delivered quality parts from our suppliers.

The Llanberis site is currently involved in new product introductions, so this is an exciting time to join an existing team of Quality professionals to help develop the future processes of the Llanberis manufacturing site. The successful applicant will report directly to the Instrumentation Quality Assurance Manager and is a member of the wider Quality Management team, collectively responsible for maintaining and improving quality & compliance in the manufacture and support of our products and services.

• Onboard new suppliers and support existing suppliers to deliver high quality parts, conduct supplier audits across our supply base in Europe, review supplier performance and drive continuous improvements through supplier performance reviews.
• Develop world-class supply chain processes to suit a low volume, high complexity multi-technology environment (diagnostic instrumentation).
• Provide key support onsite for supplier quality management services within an ISO 13485 and FDA 21 CFR Part 820 regulatory environment.
• Manage suppliers to deliver quality products to internal customers, through product & process investigations & evaluations.
• Liaise with a wide variety of external suppliers to ensure they are trained and adhere to Siemens First Articles, Quality and Regulatory requirements.
• Issue Supplier Corrective Action Reports and work with suppliers on Root Cause Investigations and Corrective Action.
• Conduct Supplier Performance Reviews and report key supplier quality metrics.
• Ensure timely closures of non-conformities and SCARS.
• Work closely with procurement on a day‑to‑day basis.

• Ideally with a minimum of 2 years relevant experience in a Quality Engineering role.
• Minimum of a third level qualification (Diploma/Degree) in an appropriate discipline (Quality Management, Mechatronics, Electronics or Mechanical Engineering) or equivalent experience.
• Experience leading and being part of teams and projects with strong written and verbal communication skills.
• Ability to work in technically complex multi‑discipline areas across the whole supply chain, including the supplier environment.
• Knowledge of inspection methodologies such as fabricated/machined metal mechanical/visual inspection, precision linear measurement, non‑contact measurement, molded and machined plastics inspection and measurement.
• Excellent oral and written communication skills.
• Lead auditing experience with ISO 9004:2015 and ISO 13485:2016.
• Ideally have a working knowledge of Six Sigma, statistical analysis and Lean principles for investigations, problem solving and continuous improvement.

• 26 days' holiday with the option to buy or sell an additional 5
• Up to 10% employer pension contribution
• Share and bonus scheme
• Access to our flexible benefits from private medical insurance to dental cover
• Corporate Social Responsibility opportunities including 2 paid volunteering days per year and support from our 24/7 employee assistance programme

We are a team of more than 71,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision‑making and treatment pathways.

When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare.

For everyone. Everywhere. Sustainably.

As an equal opportunity employer, we welcome applications from individuals with disabilities.

We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. Please create a profile within our talent community and subscribe to personalized job alerts that will keep you posted about new opportunities.