Hybrid Pharmaceutical Quality GCP Auditors – Consulting

Posted 3 weeks ago

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About the role

  • Auditor supporting compliance reviews for GCP projects based in Israel. Conducting audits and preparing reports for clinical trial sites and vendors.

Responsibilities

  • Conduct Good Clinical Practice (GCP) audits (planning, agenda, physical or remote audit, and report writing)
  • Evaluate investigator sites, CROs, and vendor compliance or qualification.
  • Prepare comprehensive audit reports detailing findings and root-causes.
  • Provide written audit reports in English.
  • If required will provide corrective actions support and present findings to QA leadership and stakeholders
  • Work collaboratively with clients to ensure quality standards.

Requirements

  • Minimum 10+ years of Clinical Quality Assurance and/or Good Clinical Practice (GCP) experience.
  • Minimum 5+ years of Good Clinical Practices auditing experience.
  • Demonstrated experience with regulatory agency expectations (e.g., FDA, EMA) and audit readiness activities.
  • Demonstrated experience in developing and implementing quality assurance plans, audit programs, and corrective action plans.
  • B2 level in English communication, verbal and written
  • B2 level in Hebrew communication, verbal and written
  • Bachelor's degree

Benefits

  • Flexible work arrangements
  • Professional development

Job title

Pharmaceutical Quality GCP Auditors – Consulting

Job type

Experience level

SeniorLead

Salary

Not specified

Degree requirement

Bachelor's Degree

Location requirements

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