Supports the development and execution of assigned project elements focused on manufacturing processes, technology, and procedures for new product introductions. This role offers the opportunity to learn and apply engineering techniques in a regulated manufacturing environment, helping to accelerate product time to market while ensuring quality and compliance.

• Support and executes assigned project elements with an emphasis on manufacturing systems and procedures.
• Assist in project planning and coordination efforts in line with best practices in project management.
• Provide technical/engineering support for new product and process introductions, contributing to documentation in accordance with Stryker’s Design Transfer and Design Control procedures.
• Ensure quality of process and product as defined in the appropriate operation and material specifications.
• Will assist in the selection of components and equipment based on analysis of specifications, reliability and regulatory requirements. Work with quality engineers to develop component specific testing and inspection protocols.
• Support capital acquisition activity from specifying equipment, contract negotiation, Installation and validation.
• Will analyse equipment to establish operating data, conduct experimental test and result analysis. Lead and/or participate in process review meetings.
• Participate in PFMEA, Control Plan, SOP and PPAP generation associated with product transfers and launches.
• Will inspect parts that third party suppliers and sites manufacture and assess how they compare to the intended specification.
• Complete capability studies for in process inspection and generate subsequent Inspection documentation.
• Conduct MSA studies for new products and new processes.
• Provide training for manufacturing team members.
• Ensure adherence to GMP and safety procedures.
• Review and approval of validation documentation.
• All other duties as assigned.

• B.S. in Mechanical Engineering or a related engineering discipline.
• Up to 1 year of relevant industry or internship experience desirable (placement/internship experience acceptable).
• Self-starter with demonstrated efficient work methods, analytical & problem-solving skills and ability to handle multiple tasks in a fast-paced environment.
• Proactive and eager to learn, with good problem-solving and organizational skills.
• Team player with strong interpersonal and communication skills.
• Basic understanding of manufacturing processes and engineering drawings (training will be provided).
• Familiarity with Microsoft Office and general PC skills required.
• High attention to detail and willingness to adhere to standards and documentation practices.
• Knowledge of medical device or regulated industries is a plus but not required.

Posted Date: 01/13/2026
This role will be posted for a minimum of 3 days.