Associate Manager, Quality Assurance

Posted 2 Days Ago
Be an Early Applicant
Irvine, CA, USA
In-Office
116K-193K Annually
Senior level
Healthtech
The Role
Leads a Quality Operations and Quality Engineering team in a regulated manufacturing environment. Oversees compliance with quality standards and regulatory requirements, audits, inspections, quality systems, nonconformances, CAPAs, deviations, and risk mitigation. Drives continuous improvement, monitors quality metrics, supports product and process quality, and recruits, develops, and retains high-performing talent while partnering with manufacturing and cross-functional leaders.
Summary Generated by Built In
Work Flexibility: Onsite

Stryker is hiring an Associate Manager, Quality Assurance in Irvine, CA to lead a high-performing Quality Operations team and drive quality excellence across manufacturing and business functions. In this role, you will provide leadership and direction for quality assurance activities with a strong focus on compliance, risk prevention, continuous improvement, and operational effectiveness. You will be responsible for ensuring adherence to Stryker Corporate and SGS requirements, Quality System Regulations, and applicable industry standards while fostering a culture of engagement, accountability, and quality ownership. This position plays a key role in delivering both compliance and business objectives, supporting product quality, process improvements, and overall organizational success.

What you will do:

  • Lead and develop a Quality Engineering team, providing guidance and support to manufacturing and cross-functional partners while promoting a culture of quality and continuous improvement.
  • Ensure products, processes, and systems comply with Stryker quality standards, regulatory requirements, and customer expectations.
  • Foster an inclusive, engaged, and high-performing team environment through coaching, development, and effective employee relations practices.
  • Recruit, develop, and retain talent, aligning team strengths with business needs and future growth opportunities.
  • Partner with site leaders and functional teams to establish, maintain, and improve quality systems, standards, and compliance processes.
  • Support internal, external, and regulatory audits, helping maintain site certifications and inspection readiness.
  • Oversee investigations, nonconformances, CAPAs, and product/process deviations, ensuring timely resolution and effective risk mitigation.
  • Monitor quality performance metrics and drive quality improvement initiatives that enhance product quality, reduce risk, improve efficiency, and support site and global business objectives.

What you need:

Required

  • Bachelors degree in Engineering or Science related discipline.
  • Minimum of 6+ years’ experience in a Medical, Pharmaceutical, Bio-Medical/Pharma, Automotive or regulated manufacturing environment.
  • Expert working knowledge of regulatory requirements, standards and regulations, with experience of managing inspections/audits by governing and/or regulatory bodies.
  • Working knowledge of quality tools such as SPC / Process Control, FMEA, Problem Solving / Root Cause Analysis, Poka-Yoke, or other Six Sigma tools.

Preferred

  • Experience working within FDA-regulated medical device, pharmaceutical, or life sciences environments preferred.
  • Business Management or MBA is an advantage.
  • Demonstrated success in building, leading, and developing high-performing, engaged teams is preferred.
  • Demonstrated ability to execute organizational and functional strategies while leading and driving change initiatives, with a proven track record of influencing and implementing change at both the individual and team levels.

  


US30: $116,100 - $193,400 USD Annual

  


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 or a Science-related discipline
  • At least 6 years of experience in a medical, pharmaceutical, biomedical/pharmaceutical, automotive, or regulated manufacturing environment
  • Expert working knowledge of regulatory requirements, standards, and regulations
  • Experience managing inspections or audits by governing or regulatory bodies
  • Working knowledge of quality tools such as SPC, process control, FMEA, root cause analysis, Poka-Yoke, or other Six Sigma tools
  • Experience in FDA-regulated medical device, pharmaceutical, or life sciences environments
  • Business Management or MBA
  • Demonstrated success building, leading, and developing high-performing, engaged teams
  • Ability to execute organizational and functional strategies, lead change initiatives, and influence change at individual and team levels

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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