Senior Manufacturing Engineer- Neurovascular in Salt Lake City, UT at Stryker Corporation

发布日期: 2/17/2020



Stryker is one of the world’s leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. Stryker offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives.

We are currently seeking a Senior Manufacturing Engineer to supporting Stryker’s global quality and operations team in Salt Lake City, Utah.

As the Senior Manufacturing Engineer, you will be supporting manufacturing for Stryker’s Neurovascular Product Line.  

Who we want:

Detail-oriented process improvers. Critical thinkers who naturally see opportunities to develop and optimize work processes – finding ways to simplify, standardize and automate.

Meticulous documenters. Detail-oriented people who enjoy maintaining meticulous documentation of reports, metrics, proposals, and presentations.

Self-directed innovators. People who take ownership of their work and need no prompting to drive productivity, change, and outcomes.

Strategic thinkers. People who enjoy analyzing data or trends for the purposes of planning, forecasting, advising, budgeting, reporting, or sales opportunities.

Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in functions.

What you will do:

As Senior Manufacturing Engineer, you will be responsible for directing and coordinating fabrication, installation, operation, application, maintenance and repair of mechanical or electromechanical machines, equipment, tools, engines and systems.

You will be responsible for ensuring that quality levels and industry standards are maintained or improved in the manufacturing process. As the Senior Manufacturing Engineer, you will oversee installation, operation, maintenance and repair of equipment such as centralized heat, gas, water and steam systems. You will evaluate mechanical products to determine their cost effectiveness and efficiency. You may also evaluate field installations and recommend design modifications to eliminate malfunctions.

Additional responsibilities include:  

  • Design, document, and improve manufacturing processes and operations that control the safety and efficacy of finished devices.
  • Conduct qualification, verification, and validation activities for the production of medical devices.
  • Analyze, troubleshoot and resolve issues relating to the safety, efficacy, quality, cost, or delivery of components and finished devices.     
  • Complete engineering work and contribute to new product development teams and product support, typically including the following activities: technology development, test of materials or products, preparation of specifications, Six Sigma, process study, process improvements, and report preparation.
  • Design & develop manufacturing equipment in compliance with manufacturing safety (e.g., OSHA & EPA) principles.
  • Design, procure, and fabricate tooling and fixtures.
  • Participate in design control efforts related to risk analysis (FMEA) & design reviews.
  • Train, develop, and/or provide work direction to operators and technicians.
  • Participate in the identification, implementation, and management of production goals.
  • Participate on cross-functional project teams. Coordinate, manage, and document project work and progress, and recommend appropriate revisions.
  • Design and coordinate engineering tests and experiments. Analyze data, draw conclusions, and summarize test results. Communicate results to manager.
  • Interfaces with product builders or extrusion technicians, production supervisors, and engineers in troubleshooting problems on the production floor.

Participates in project teams typically including one of the following:

  • Identifying and implementing process/product improvement alternatives to increase/optimize yield, efficiency, throughput, and/or performance.
  • Designing, performing, and documenting engineering test experiments to evaluate product/process performance.
  • Designing, developing, testing, and validating equipment and processes; analyzing and interpreting process models and recommending process improvements.
  • Evaluating external process technologies.
  • Coordinates with the appropriate suppliers and other external resources needed in developing and implementing process/product improvement plans.
  • Participates in project planning and scheduling.
  • Attends and contributes to production core team meetings.

What you need:

  • Bachelor’s degree in engineering required. (Mechanical, Manufacturing, Biomedical preferred).
  • 2+ years related work experience required.
  • 2+ year manufacturing engineering preferred.
  • Medical Device experience highly preferred.

Work From Home: Not available

Travel Percentage: 10%

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.