Job Detail

Senior Supplier Quality Engineer

inApply with LinkedIn ®|more

Requisition Number

EMEA05167

Employment Type

Full-time

Location

Winterthur

Founded in 1927 and headquartered in Warsaw, Indiana, USA, Zimmer Biomet is a global leader in musculoskeletal healthcare. We design, manufacture and market orthopaedic reconstructive products; sports medicine, biologics, extremities and trauma products; spine, bone healing, craniomaxillofacial and thoracic products; dental implants; and related surgical products.

We collaborate with healthcare professionals around the globe to advance the pace of innovation. Our products and solutions help treat patients suffering from disorders of, or injuries to, bones, joints or supporting soft tissues. Together with healthcare professionals, we help millions of people live better lives.

For the European Headquarters, based in Winterthur (Switzerland), we are looking for a

 

Senior Supplier Quality Engineer

This position is announced in the Supplier Quality Life cycle Team which is a team within the Supplier Quality Assurance (SQA) department at Zimmer Biomet Winterthur.

 

Your main Responsibilities:

• Support the overall Supplier Quality Management


• Supporting the implementation of the new Medical Device Regulation (MDR)


• Perform the Supplier Production Part Approval Process (SPPA) including the approval and release of suppliers activities such as supplier validation documents and records


• Perform Supplier Audits as Lead Auditor and participate in Audits at Zimmer Biomet Winterthur


• Analyzing, improving and writing procedures related to Supplier Quality Assurance


• Assists suppliers in developing strategies for corrective and preventive actions


• Focus on New Product Introduction (NPI) and Manufacturing Transfers

Your Qualifications and Experience:

• Bachelor or Master in Engineering or Natural Science (university degree and/or higher technical education)


• Five (5) or more years of experience in Medical Device Industry (Class III, II and I medical devices)


• Broad knowledge of standards and regulations as ISO 13485:2016, 21 CFR Part 820, Medical Device Directive (MDD), Medical Device Regulation (MDR), etc.


• Strong skills in validation in the Medical Device Industry including risk analysis and measurement system analysis.


• Ability to work in an interdisciplinary environment with interfaces to other departments and to customers


• Lead Audit Certification preferred


• Fluent in English and German

Travel Requirements:

Up to 15%.

If you seize this opportunity, you will be able to develop your international experience and be a part of a great and truly global team. Zimmer Biomet offers a wide range of challenging career advancement opportunities and a dynamic work environment. We look forward to receiving your complete application online.

 

Zimmer GmbH

Cenk Korkmaz

Human Resources

Tel: +41 58 854 84 68

www.zimmerbiomet.com

[Close][Email a friend](Please note: this link will open the page in a new browser window.)[Print][Apply for job](Please note: this link will open the page in a new browser window.)|more