As a member of the Technical Office team you will gain in depth knowledge about Stryker’s Trauma & Extremities portfolio. You will learn how External Fixators, Bone Plates & Screws, Surgical Instruments and many other products improve people’s life.
Together we are responsible for over 10'000 articles. We count on you to maintain and improve our high standard in design specification and performance.
You oversee the continuous improvement projects for existing products in our group, create and manage project plans, assign and follow up on work packages. You participate in and at times lead cross functional teams to perform design related Non-Conformities(NC), Corrective- and Preventive-Actions(CAPA).
In your field of responsibility, you will make sure that design requirements are met as well as apply the design change process and identify technical solutions in this context.
Your role will include frequent contact with other teams such as the international Regulatory Affairs, Tech. Publications, Design Quality or Marketing to address design related questions for international registrations and creations of technical files required for the implementation of EU-MDR requirements.
Your profile
You have undergone a technical education, are qualifying as engineer (HF, FH, Uni, ETH) and have gained 5+ years professional experience in product development, -care or -surveillance.
Desirably you bring experience working in the medical device industry and knowledge of the applicable regulations and design controls.
Apart from excellent project management skills you have developed technical understanding and are familiar with design specifications and drawings.
You are characterized by analytical reasoning, a focused and pro-active work style along with a high sense of responsibility, persistence, advanced problem solving and people skills.
You value an international working environment where you can use your good command of English and German.
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