Senior Quality Engineer in Fremont, CA at Stryker Corporation

Date Posted: 2/9/2020

Job Snapshot

Job Description

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. The Company 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 Quality Engineer located in Fremont, California

Who we want:

Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.

Goal-oriented developers. Keeping the customer and system requirements squarely in focus, people who deliver safe and robust solutions.

Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, information, use cases, and industry analyses to develop best practices.

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

What you will do:

  • Will work within the Quality Systems team, under general supervision, with responsibility to ensure an effective and efficient quality management system is maintained. This includes, but not limited to, the following:
  • Support the ongoing management of Contract Manufacturer and Original Equipment Manufacturer activities
  • Support the optimization of Quality Systems to facilitate the efficient integration of company or product acquisitions
  • Have responsibility for review and approval of NC and CAPAs. Liaise with relevant functional groups to facilitate and mentor teams through all stages of the NC / CAPA process. Administer process for product holds and rework associated with NC’s.
  • Coordinate Quality Planning process and metrics
  • Execute Change Management per global/corporate systems requirements.
  • Performs responsibilities required by the Quality System and other duties as assigned or requested.

What you need:

  • BA/BS in Engineering or related discipline.
  • 3+ plus years of overall medical device experience
  • Experience with supplier quality management systems
  • NC/CAPA experience
  • Quality System integration experience preferred
  • Strong written/verbal communication skills.
  • Demonstrated used of problem-solving tools/methodologies
  • Demonstrated experience with continuous improvement projects
  • Lean 6 Sigma certification is desirable
  • ASQ or other professional certification preferred
  • Experience in working on multi-disciplinary teams
  • Ability to successfully interface with various departments and personnel
  • Ability to work independently and motivated to perform at a high-level without constant supervision
  • Ability to handle multiple projects on an ongoing basis
  • Ability to adhere to necessary processes within a regulated environment

Work From Home: Occasional

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.

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