SUPPLIER QUALITY ENGINEER

We are currently looking to strengthen our Quality Assurance organization with a Supplier Quality Engineer (SQE) within Dentsply Sirona Implants. The position is located at our site in Mölndal, Sweden and report directly to the Head of Quality Assurance.

Dentsply Sirona is the world´s largest manufacturer of professional dental products and technologies, empowering dental professionals to provide better, safer and faster dental care. Our products and solutions include leading positions and platforms across consumables, equipment, technology, and specialty products. Dentsply Sirona´s Global Headquarters is located in York, Pennsylvania, and the International Headquarters is based in Salzburg, Austria. Our shares are listed in the United States on NASDAQ under the symbol XRAY, and in the 12 months ended December 31, 2015, the combined company had pro-forma revenue of approximately $4 billion. More information about Dentsply Sirona and its Products can be found at www.dentsplysirona.com.

DESCRIPTION
As SQE at Dentsply Sirona Implants you will work closely with the Global Purchasing department and our suppliers. The main objective for the position is to secure Quality Assurance of supplied components/products. Production Part Approval Process (PPAP) is used as the tool for Quality Assurance. The SQE will work in a Global Environment and be part of cross functional teams. In order to secure fulfilment of established requirements and be able to solve any issues close cooperation with other functions as well as close cooperation with SQE in Sweden and Germany is required.

You will in your daily work be responsible for:
- Fulfilment of PPAP elements
- Design reviews with the supplier in order to transfer knowledge of the components/products
- Performing Supplier Audits according to ISO 13485
- Supplier Nonconformities and CAPA

QUALIFICATIONS
For this role in a truly global business environment, we look for qualified candidates with a relevant background. The position requires a university degree in engineering or an equivalent professional background. Experience of working with PPAP for several years and qualified to act as lead auditor is a requirement. If you have experience from working in medical device industry and have knowledge about ISO 13485 it is an advantage.
Personal characteristics are analytical skills, attention to details and the ability to work both in cross functional team and independently. We believe that you are a positive and social person with the ability to maintain a good relation with both external and internal contacts. It is an advantage if you have strong focus and drive to achieve goals and targets.

INFORMATION
For more information, please contact Christina Pettersson, recruiting manager, phone +46-(0)31-376 31 22.

We need your application no later than June 12th 2016. Please note that we will review applications continuously, so be sure to send in your application as soon as possible.

Welcome with your application!