Onsite
Full Time Posted 3 hours ago
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Job Details

What you will do-

  • 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).
  • Develop and execute end-to-end change management plans aligned to OnePLM (CAI, CAII and CAIII) and engage in the development of optimum future state of QMS for business needs.
  • Identify improvements and inputs into the quality planning process; execute development and/or modification of Stryker's QMS and support Management Review and Quality Planning Review and related forums, GMP and GDP within Quality organization.
  • Assess and quantify requirements for QMS requirements to optimize structure.
  • Identify and implement improvement opportunities to increase the efficiency and effectiveness of the QMS.
  • Support implementation of best-in-class practices and benchmark against industry leaders and regulatory requirements and notified body communication; internal and external quality system audits; change control assessment and approval.
  • Ensure QMS reflects actual activities, business needs and supports NPD requirement.
  • Basic project management understanding and system integration.
  • Key contributor to QMS business process(es) and support requirements.

What you will Need-

Required:

  • BS in a science, engineering, business or related discipline.
  • Experience - 2 years - 5 years in manufacturing environment or equivalent.

Preferred:

  • Knowledge and understanding of US and International Medical Device Regulations.
  • Advanced proficiency in Excel (pivot tables, complex formulas, data analysis) and Power BI (dashboards, reporting)
  • Basic knowledge of Quality Systems (CAPA, audits, Management Review, Quality Planning, etc.); communication and project management skills.
  • Strong interpersonal skills, written, oral communication and negotiations skills; Basic analytical and problem-solving capabilities.
  • Demonstrated ability to work in cross-functional team environments.
  • Some travel may be required.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
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Quality Engineer
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