Hourly Adverse Event Reporting Jobs in Riverside, CA

Job Summary

The Clinical Complaint Specialist is responsible for the clinical assessment, evaluation, and processing of medical device complaints in support of regulatory compliance and product safety activities. This role applies clinical expertise to evaluate complaint events, assess potential patient impact, determine regulatory reportability, support investigations, and ensure accurate complaint documentation. The Clinical Complaint Specialist partners cross-functionally to support complaint handling, post-market surveillance, and continuous improvement initiatives.

Please note this position is on site full time and based in Irvine, CA. 

Duties & Responsibilities

• Review, evaluate, and process medical device complaints in accordance with applicable regulations, company procedures, and quality system requirements.
• Perform clinical assessments of complaint events to determine severity, potential patient impact, and device-relatedness.
• Evaluate complaints for regulatory reportability, including Medical Device Reporting (MDR), vigilance reporting, and other applicable global adverse event reporting requirements.
• Classify and code complaint events using established coding systems and internal procedures.
• Review complaint records for completeness and obtain additional information as necessary to support complaint evaluations and investigations.
• Document complaint assessments, reportability determinations, and supporting rationale within complaint management systems.
• Support the preparation, review, and submission of adverse event reports to regulatory authorities as required.
• Collaborate with Quality, Regulatory Affairs, Medical Affairs, Clinical Affairs, Engineering, Manufacturing, and other cross-functional teams to support complaint investigations and resolution activities.
• Identify and escalate potential product safety concerns, emerging risks, and quality issues.
• Participate in post-market surveillance activities, including complaint trending, signal detection, and risk assessments.
• Support internal audits, regulatory inspections, and quality system assessments related to complaint handling processes.
• Assist with the development, maintenance, and continuous improvement of complaint handling procedures, work instructions, and quality system documentation.
• Maintain current knowledge of applicable regulations, standards, and industry best practices related to complaint handling and post-market surveillance.
• Perform other duties as assigned.

Minimum & Preferred Qualifications and Experience: 

Minimum Qualifications

• Registered Nurse (RN), Bachelor of Science in Nursing (BSN), or equivalent clinical degree.

• Minimum three (3) years of clinical nursing or direct patient care experience.

• Strong clinical assessment and critical thinking skills.

• Ability to interpret medical records, clinical documentation, and adverse event information.

• Strong written, verbal, and interpersonal communication skills.

• Strong attention to detail and organizational skills.

• Proficiency with Microsoft Office applications.

Preferred Qualifications

• Experience in the medical device, biotechnology, pharmaceutical, diagnostics, or healthcare industry.

• Experience with complaint handling, adverse event reporting, post-market surveillance, or quality systems.

• Knowledge of FDA Medical Device Reporting requirements (21 CFR Part 803), complaint handling requirements (21 CFR Part 820), and applicable international vigilance regulations.

• Experience using electronic quality management systems (eQMS) or complaint management systems.

• Advanced clinical degree or specialty certification.

Education

• Registered Nurse (RN), Bachelor of Science in Nursing (BSN), or equivalent clinical degree required.
• Advanced clinical degree or specialty certification preferred.

Compensation:

The anticipated salary range for this position is $80,000 - $100,000 plus benefits.  Actual placement within the range is dependent on multiple factors, including but not limited to skills, education, and experience. 

This position also qualifies for up to 10% annual bonus based on Company, department, and individual performance. 

 Masimo offers benefits such as Medical, Dental, Vision, Life/AD&D, Disability Insurance, 401(k), Vacation, Sick, Holiday, Paid Maternity Leave, Flexible Spending Accounts, Voluntary Accident, Critical Illness, Hospital, Long-Term Care, Employee Assistance Program, Pet Insurance, On-site wellness clinic, fitness center, and cafe.  All benefits are subject to eligibility requirements.

Language requirements

• Ability to read, write, and communicate effectively in English.
• Ability to interpret technical documents, schematics, and written instructions.
• Ability to clearly document technical findings and communicate with cross-functional team members.

Physical requirements/Work environment

This position primarily works in an office environment and requires frequent sitting, standing, and walking. Daily use of a computer and other digital devices is required. This role may require standing for extended periods when facilitating meetings or walking through facilities.

The physical demands of the position described herein are essential functions of the job and employees must be able to successfully perform these tasks for extended periods.  Reasonable accommodations may be made for those individuals with real or perceived disabilities to perform the essential functions of the job described.

Masimo is proud to be an EEOE/, M/F/D/V, and we are committed to Diversity at the corporate level.