Senior Quality Management Systems Specialist in Elstree at Stryker Corporation

掲載日付: 8/22/2019



  • Supports QMS compliance with the appropriate internal and external regulatory requirements (including but not limited to Site, Division, Corporate, FDA, ISO, MDD, and individual country requirements).
  • Contribute to the development of optimum future state of QMS for business needs.
  • Oversee and execute development and/or modification of Stryker's QMS.
  • Lead change management process for the site
  • Assess and quantify requirements for QMS requirements to optimize structure.
  • Drive GMP and GDP within Quality organization.
  • Identify and implement improvement opportunities to increase the efficiency and effectiveness of the QMS.
  • Develop and deliver training for QMS areas of expertise.
  • Contribute to the development, maintenance, and improvements of policies and procedures.
  • Implement best-in-class practices and benchmark against industry leaders and regulatory requirements.
  • Engage in relevant QMS IS discussions.
  • Key contributor to QMS business process(as) and understand IS system support requirements.
  • Understands system integration.
  • Support IS change control assessment and approval.

Work From Home: No

Travel Percentage: Up to 25%