Product Complaint Specialist jobs in United States
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Stryker · 1 day ago

Product Complaint Specialist

Stryker is hiring a Product Complaint Specialist in Irvine, CA! In this role, you will drive accurate and timely complaint processing that ensures device performance meets global standards, transforming data into action and supporting continuous improvement across devices and quality systems.

BiotechnologyHealth CareLife ScienceMedicalMedical Device
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Growth Opportunities
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H1B Sponsor Likelynote

Responsibilities

Review product documentation, analyze trending data, and submit required information to support compliant complaint processing
Maintain complete and accurate complaint records in alignment with U.S. and international regulatory requirements
Process customer complaints within defined timelines and ensure all required information is collected and documented for regulatory decision‑making
Assess clinical and technical information to support thorough investigations, root‑cause analysis, and quality engineering review
Prepare customer response letters and support clear, timely communication with internal teams
Assist during FDA and Notified Body inspections by providing documentation and process expertise
Coordinate and participate in cross‑functional meetings with Engineering, R&D, Marketing, Customer Service, and Technical Services
Generate reports to support rapid review of new complaints, regulatory submissions, and follow‑up actions
Escalate product trends and potential issues to appropriate stakeholders for evaluation and disposition
Conduct failure analysis on returned devices as required and apply device risk‑management knowledge to complaint evaluations

Qualification

Quality management systemsComplaint handlingRegulatory reportingEngineering backgroundData analysisRoot-cause analysisCommunication skills

Required

Bachelor's degree required. Focus on Engineering, Science, or a related field is beneficial
Minimum 0 years' experience

Preferred

Internship experience in quality, engineering, manufacturing, or related technical functions within regulated industries is strongly preferred
Knowledge of quality management system concepts, including good documentation practices, corrective and preventive action processes, and document control
Experience supporting complaint handling or quality engineering in medical devices
Familiarity with regulatory reporting requirements such as Medical Device Reporting under 21 CFR 803

Benefits

Bonus eligible
Benefits

Company

Stryker is a medical technology company that offers products and services in orthopaedics.

H1B Sponsorship

Stryker has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (105)
2024 (76)
2023 (63)
2022 (78)
2021 (57)
2020 (77)

Funding

Current Stage
Public Company
Total Funding
unknown
1990-01-02IPO

Leadership Team

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Kevin Lobo
Chair & CEO
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Glenn S. Boehnlein
Chief Financial Officer and Vice President
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Company data provided by crunchbase