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Stryker

Manufactures orthopedic and surgical medical devices

Manager Quality Engineering

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeMahwah, NJ, USA$141.6k - $236k /yrIn-person

About the Job

Requirements

  • A bachelor's degree in Engineering, Quality, Life Sciences, Manufacturing, or a related technical discipline.
  • At least 6 years of experience in a technical, manufacturing, quality, or engineering role within a regulated industry.
  • At least 3 years of experience leading teams, projects, or quality management activities.
  • Experience working within a regulated manufacturing environment, including compliance with FDA and/or international quality standards.
  • Experience supporting quality systems, audits, investigations, corrective actions, and process improvement initiatives.

Responsibilities

  • Lead the Quality Assurance team, providing technical guidance and quality oversight across manufacturing and operations support functions to drive continuous improvement and compliance.
  • Partner with site leadership to ensure products consistently meet customer expectations, regulatory requirements, and applicable quality standards.
  • Develop, coach, and retain a high-performing team while fostering a culture of inclusion, accountability, collaboration, and employee engagement.
  • Drive quality system compliance by partnering with functional leaders to establish, communicate, and maintain quality standards, requirements, and responsibilities.
  • Lead site readiness activities and support internal, corporate, notified body, FDA, and other regulatory audits and inspections.
  • Oversee management of nonconforming products, product and process deviations, risk assessments, corrective actions, and preventive actions to ensure effective resolution and compliance.
  • Monitor and improve Quality performance indicators, including NCR, CAPA, compliance, and operational quality metrics, and implement corrective actions for adverse trends.
  • Support development and execution of local and global Quality Operations strategies that improve product quality, operational efficiency, risk management, and regulatory compliance.

Desired Qualifications

  • A master's degree in Business Management, Engineering, or Science, or an MBA.
  • Experience leading and developing high-performing quality teams in a manufacturing environment.
  • Experience establishing quality strategies and performance improvement programs across multiple sites or business units.
  • Black Belt, Green Belt, or equivalent Lean/Six Sigma certification.
  • Experience supporting global quality systems, regulatory compliance initiatives, and continuous improvement programs.
  • Experience influencing cross-functional stakeholders and driving quality culture initiatives.

About the Company

Stryker

Manufactures orthopedic and surgical medical devices

Stryker makes medical devices for hospitals, surgical centers and emergency responders, spanning joint implants, surgical instruments and patient transport equipment. Its Mako platform assists surgeons with joint replacement, while its neurotechnology products support brain and spine procedures and stroke treatment. Clinicians use its equipment during surgery and emergency care, and the company earns money by selling implants, disposable products and capital equipment through direct sales teams and distributors. The business also supplies training and technical support for healthcare providers using its devices. Stryker was founded in 1941 and is headquartered in Portage, Michigan.

Company size
10,001+
Company stage
IPO
Headquarters
Portage, MI
Founded
1941

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