Manager, Quality Engineering

Posted 6 Days Ago
Be an Early Applicant
Mahwah, NJ, USA
In-Office
142K-236K Annually
Senior level
Healthtech
The Role
Lead site Quality Assurance activities across regulated manufacturing operations. Manage quality systems, audit readiness, nonconformances, deviations, risk assessments, CAPA, investigations, and quality performance metrics. Partner with Operations, Regulatory Affairs, Global Quality, suppliers, and site leadership to ensure compliance, improve processes, and maintain product quality. Lead, coach, and develop the Quality Assurance team while supporting regulatory audits and continuous improvement strategies.
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 FDA and/or international quality standards
  • Experience supporting quality systems, audits, investigations, corrective actions, and process improvement initiatives
  • 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

Inari Medical Compensation & Benefits Highlights

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

  • Fair & Transparent Compensation — Pay is considered competitive for many roles, with employees described as 'extremely happy' with total compensation including pay, stock, equity, and benefits. Feedback suggests above‑average salary levels across departments contribute to strong pay sentiment.
  • Healthcare Strength — Benefits include comprehensive medical, dental, and vision coverage, with 100% employer‑paid premiums for employees cited in multiple descriptions. Additional options like critical illness, accident, hospital indemnity, and wellness programs reinforce the healthcare offering.
  • Leave & Time Off Breadth — Time off is characterized by unlimited PTO, cited as a top benefit by employees. Paid holidays and flexible hours are also referenced, expanding the range of time‑off options.

Inari Medical Insights

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The Company
HQ: Irvine, CA
956 Employees

What We Do

Inari Medical, Inc. is a commercial-stage medical device company focused on developing products to treat and transform the lives of patients suffering from venous diseases.

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