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Job description
Stryker is hiring a Senior Engineer, Product Development in Mahwah, New Jersey, to support Joint Replacement! In this role, you will research, design, validate, and contribute to bringing new products to market!
Work Flexibility: Hybrid. This role requires reasonable proximity to our Stryker facility. You should be comfortable working two to three days onsite. This will depend on the project.
What you will do:
Technical Responsibilities:
Under minimal supervision, research, design, develop, modify, and verify components/modules for medical devices.
Translate design inputs to engineering specifications and produce sub-system level designs.
Develop and analyze solutions, prototyping one or more options to provide proof of concept.
Apply fundamental and advanced concepts, practices and procedures for problem solving.
Business Responsibilities:
Demonstrate advanced understanding of customer needs and design inputs.
Demonstrate proficiency with product’s intended use and clinical procedures.
Learn how financial models are constructed.
Med Device Compliance:
Adhere to industry standards, design requirements, and test strategies applicable to regulatory requirements.
Independently create or refine engineering documentation, such as the Design History file.
Follow R&D procedure like design controls and risk management, per the Quality Management System.
General Responsibilities:
Cross functional collaboration across R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success while solidifying relationships.
Quickly process and assimilate procedures, policies, processes, systems, and technology required.
Tackle complex problems by leveraging advanced experience and learnings.
What you need:
Required
Bachelor of Science in Engineering required. Preferred to be Mechanical Engineering, Biomedical Engineering, or Materials Science.
2+ years of related experience.
Preferred:
Working knowledge and understanding of mechanical engineering practices and design principles.
Technical ability to create engineering drawings and models, applying GD&T and CAE tools.
Demonstrated ability to apply knowledge of materials and manufacturing processes to product design.
Ability to communicate basic plans and technical information to team members.
Experience with a parametric CAD design package. Creo preferred.
Experience in FDA-regulated or highly regulated industry preferred.
Exhibit a strong sense of ownership and the ability to prioritize tasks effectively.