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.