Manager, Quality Engineering

Posted 6 Days Ago
Be an Early Applicant
Mahwah, NJ, USA
In-Office
142K-236K Annually
Senior level
Healthtech • Other • Robotics • Biotech • Manufacturing
Together with our customers, we're on a mission to make healthcare better.
The Role
Leads site Quality Assurance activities across regulated manufacturing and operations. Manages quality systems, audit readiness, FDA and regulatory inspections, nonconforming products, deviations, risk assessments, CAPA, and quality performance metrics. Partners with Operations, Global Quality, Regulatory Affairs, suppliers, and site leadership to ensure compliance, product quality, continuous improvement, and operational effectiveness. Also develops and coaches the Quality Assurance team.
Summary Generated by Built In
Work Flexibility: Onsite

As the Manager, Quality Assurance, you will lead quality assurance activities that support product quality, process performance, audit readiness, and continuous improvement across site operations. Working closely with Operations, Global Quality, Regulatory Affairs, and supplier partners, you will help ensure quality systems remain effective, compliant, and aligned with business objectives. This role is Onsite in Mahwah, New Jersey.


What You Will Do
  • Lead the Quality Assurance team, providing technical guidance and quality oversight across manufacturing and operations, supports 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 the 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 the development and execution of local and global Quality Operations strategies that improve product quality, operational efficiency, risk management, and regulatory compliance.

What You Need
  • Bachelor’s degree in Engineering, Quality, Life Sciences, Manufacturing, or a related technical discipline.
  • Minimum 6 years of experience in a technical, manufacturing, quality, or engineering role within a regulated industry.
  • Minimum 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.

Preferred Qualifications
  • Master's degree in Business Management, Engineering, 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.

  


United States of America Pay Ranges:


  • US20: $141,600 - $236,000 USD Annual

View the U.S. work location and transparency guide to find the pay range for your location.


  


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.

Skills Required

  • 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.

Stryker Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Stryker and has not been reviewed or approved by Stryker.

  • Healthcare Strength — Multiple medical plan options with HSA support and global mental‑health access indicate broad, accessible care. These features materially enhance the overall value of the total‑rewards package.
  • Retirement Support — A meaningful 401(k) company match with potential additional company contribution, alongside an ESPP, supports long‑term savings and wealth building. Documented plan specifics help employees understand eligibility, timing, and vesting mechanics.
  • Parental & Family Support — Paid parental and caregiver leave, adoption and surrogacy assistance, and practical supports like breast milk shipping reflect a comprehensive, family‑friendly approach. These offerings address varied family‑building paths and caregiving needs.

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The Company
HQ: Portage, MI
51,000 Employees
Year Founded: 1941

What We Do

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 130 million patients annually. More information is available at www.stryker.com. Together with our customers, we are driven to make healthcare better.

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