Quality Control Inspector

Professional
Research Triangle Park, NC

Roles & Responsibilities

  • Review and ensure the accuracy and completeness of medical records, surgical records, protocols, and study data.
  • Collaborate with staff to identify, evaluate, and recommend solutions to review and correct findings.
  • Draft study deviations in a timely manner and incorporate Study Director impact assessments.
  • Perform audits of protocol, SOP, and quality system elements to ensure compliance with GLP regulations and internal procedures.
  • Ensure preclinical in-vivo studies are compliant with GLP regulations (21 CFR Part 58) and adhere to internal quality guidelines.
  • Identify and report basic non-compliance within regulations and standards.
  • Collaborate efficiently with different groups, managing movements between various locations around the site according to stakeholder schedules.

Experience Required

  • Preferred: Bachelor’s degree with 3 years of preclinical medical device research experience, or 5 years of relevant work experience supporting preclinical research (e.g., LAR/surgical vet tech).
  • Background in data management and familiarity with medical device GLP research.
  • Demonstrated understanding in the use of calibrated equipment, controlled drugs, and GLP data collection/retention.

Skills & Certifications

  • Excellent attention to detail.
  • Strong data management skills.
  • Ability to collaborate effectively with various teams and stakeholders.
  • Proficiency in adhering to and enforcing compliance with GLP regulations and internal procedures.

Eligibilities & qualifications

  • Preferably holds a Bachelor’s degree with 3 years of experience in preclinical medical device research or 5 years of relevant work experience supporting preclinical research.
  • Demonstrated understanding of calibrated equipment, controlled drugs, and GLP data collection/retention.
  • Must be able to identify basic non-compliance within regulations and standards.
Posted 2026-01-18

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