Selzach, Switzerland
9 hours ago
Process Development Engineer (f/m/d) New Product Introduction - initially limited to 18 months
Work Flexibility: Onsite

Are you passionate about complex projects, highly technical issues and innovative manufacturing technologies?

In the Advanced Operations (AO) team, we develop manufacturing processes for medical products of the future. As an interface between product development and production, we form strong teams with our development partners in Selzach, Ireland and the USA as well as with various internal and external manufacturing areas. In doing so, we develop innovative manufacturing processes and coordinate process development for our new products.

Do you want to help shape the production of titanium screws, titanium plates and a diverse instrument set? Then become a part of AO Trauma & Extremities now!

Your key responsibilities

You are responsible for the process development of New Product Innovations from Product Development into serial manufacturing.As an experienced and assertive technical expert, you are responsible for the development and implementation of new technologies with a focus on milling, turning and inspection processes (e.g. CMM).You will support the Design Transfer project team in drawing analysis (applying DFx principals), evaluation of feasibility and economic viability as well as in the selection and definition of suitable machine and automation concepts.You work on validation concepts, create the corresponding documents and evaluate the process capability. Furthermore, you take responsibility for the associated qualification and validation activities of equipment (IQ, OQ, PQ) as well as measurement systems (MSA).You enjoy working in a global, dynamic & results oriented team environment where flexibility is essential.

What we are looking for

Technical or Bachelor degree in an engineering discipline with three or more years’ experience in a technical role. Deep knowledge about manufacturing processes is mandatory.You have knowledge in process development, project management and a good understanding of process optimization. Experience in an FDA regulated, or other regulated industry and deep understanding in GD&T, process validation and risk management beneficial. You are a creative, innovative, self-driven and open-minded communicator with excellent interpersonal skills and hands-on mentality. As a team player, you can collaborate effectively with multidisciplinary teams. Your excellent analytical skills, ability to plan, help you to organize.You possess a high-level resilience even in a fast-paced and stressful environment.Fluent in English and German.High level of PC Skills required (MS Excel, Powerpoint, MS Project).

We have signed the Diversity Charter and are proud to be part of this initiative to promote diversity in the workplace. Because diversity is important to us!
We welcome applications from people regardless of their ethnic, national, or social background, gender, disability, age, or sexual identity.

Travel Percentage: 10%

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