(Associate) Project Engineer (f/m/d) Research & Development for Product Integration and Design Transfer (limited contract for 24 in Selzach at Stryker Corporation

Date Posted: 11/5/2020

Job Snapshot

Job Description

Your key responsibilities

  • As a member of the R&D Integration team you will support remediation activities as a full project team member. You will lead verification and validation activities and take on the responsibility of integrating risk management requirements, process management requirements, and design controls of recently acquired products into Stryker’s product portfolio.

  • You will support or execute organizational project management tasks and you will collaborate proactively with the interfaces within the product development and the biomechanical department.

  • For marketed products, you will be point of contact for stakeholders such as Complaint Handling / Post Market Surveillance, Regulatory Affairs, Change Management etc.

  • In your new work environment, we can offer you the chance of becoming an expert in design control processes as well as an in-depth know-how in product risk management and requirements management processes.

  • At the beginning of your employment, you will initially face the opportunity of familiarizing yourself with our products and getting to know our procedures and best practices.

  • In the medium term, you will become established as an advisor, contributing the expertise you have gained to various development projects as a full member of the project team and helping optimize different process stages.

  • Your office can be in Selzach/Switzerland, Freiburg im Breisgau/Germany or Kiel/Germany. Please indicate your preference in your cover letter.

What are we looking for?

  • You have undergone a technical/mechanical education, are qualified as a technician (HF) or graduate engineer (FH/Uni/ETH) and have gained 2+ years professional experience in product development/care.

  • Apart from your familiarity with design control and transfer activities you easily write technical documents in a clear manner.

  • Desirably you bring experience working in the medical device industry and knowledge of the applicable regulations.

  • You are characterized by investigative reasoning, a focused and pro-active work style along with a high sense of duty and advanced problem-solving skills.

  • You value an international working environment where you can use your fluent command of English and solid German. Good knowledge of French is an advantage.

Contact: In case you have further questions regarding the position, please feel free to directly reach out to Sara Hendrickx via +49 (0)761 4888 547.

Work From Home: Remote

Travel Percentage: 0%

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