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Complaint Investigator

Complaint Investigator

CompanyAgilent Technologies
LocationAustin Metropolitan Area, TX, USA, Remote in USA
Salary$67760 – $127050
TypeFull-Time
DegreesBachelor’s
Experience LevelMid Level

Requirements

  • Bachelor’s degree in Biological Sciences or related field (e.g., Biomedical Engineering, Systems Engineering, Pharmacology, Chemistry)
  • 3 years of related experience in medical device post-market product surveillance and complaint handling
  • Strong analytical and problem-solving skills
  • Excellent written and verbal communication abilities
  • Proficient in data analysis and workflow troubleshooting, including instrumentation, arrays, and biological materials
  • Proven ability to manage and prioritize workload, meet deadlines, and work effectively in a dynamic environment
  • Exceptional organizational skills and attention to detail
  • Familiarity with ISO 13485, 21 CFR 820, 21 CFR 803, and QSR quality management system requirements and IVD products

Responsibilities

  • Review service records to identify product issues related to medical device/IVD quality complaints
  • Document comprehensive and accurate findings for each complaint investigation, including reportability assessment, root cause, conclusions, and corrective actions in compliance with regulatory requirements
  • Communicate and escalate investigation results and facilitate the decision-making process for failure investigations
  • Collaborate with cross-functional teams, including R&D, Quality, Manufacturing, Support and Service, Logistics, Regulatory Affairs, and Medical Affairs, to address product safety and quality issues
  • Support quality system investigations, including nonconformances, corrective actions, and preventive actions
  • Update and maintain complaint investigation procedures to ensure alignment with current standards and best practices
  • Conduct and facilitate product and process training sessions to enhance team competency
  • Participate in the analysis, tracking, and trending of complaints data for Global Quality and Regulatory Affairs meetings on a weekly and monthly basis and drive quality improvements
  • Provide support for global and local audits and inspections, ensuring compliance with regulatory standards and organizational requirements

Preferred Qualifications

  • Experience with SAP is preferred
  • Proficiency in Microsoft Office Products (Word, Excel, PowerPoint) or equivalent software applications is preferred