Who we want:We are looking for an Engineer who will, under minimal supervision, work with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management to ensure project success. The role involves researching, designing, developing, modifying, and verifying components/modules for medical devices. The candidate should quickly process and assimilate procedures, policies, processes, systems, and technology required.This is an individual contributor role that requires judgment in applying professional expertise and the ability to work independently with minimal supervision. Typically, a university degree or extensive practical experience is required. The role demands an understanding and application of procedures and concepts within the discipline, with attention to detail in making evaluative judgments based on factual information. A minimum of 2 years of experience is generally required.What you will do:Technical Responsibilities:Research, design, develop, modify, and verify components/modules for medical devices under minimal supervision.Translate design inputs into engineering specifications and produce sub-system level designs.Develop and analyze solutions, including prototyping multiple options to demonstrate proof of concept.Apply fundamental and some advanced concepts, practices, and procedures for problem solving.Business Responsibilities:Demonstrate an advanced understanding of customer needs and design inputs.Show proficiency with the product’s intended use and clinical procedures.Learn how financial models are constructed.Follow industry standards, design requirements, and test strategies applicable to regulatory requirements.Create or refine engineering documentation, such as the Design History File, independently.Adhere to R&D procedures like design controls and risk management, as per the Quality Management System.General Responsibilities:Work with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management teams to ensure project success, with minimal supervision.Quickly process and assimilate procedures, policies, processes, systems, and technology.Work on complex problems, applying advanced experience and learnings.Demonstrate ownership and prioritize work independently.Collaborate effectively as a key team member, strengthening relationships.Minimum Qualifications (Required):Bachelor of Science in Engineering, Mechanical Engineering, or Biomedical Engineering, with 2+ years of work experience.Preferred Qualifications (Strongly desired):Technical Skills:Understanding of mechanical engineering practices and design principles.Ability to create engineering drawings and models, applying GD&T and CAE tools.Knowledge of materials and manufacturing processes relevant to product design.Ability to communicate technical plans and information to team members.Stryker is a global leader in medical technologies, committed to making healthcare better through innovative products and services in MedSurg, Neurotechnology, Orthopaedics, and Spine. The company impacts more than 150 million patients annually worldwide.
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