Hybrid Pharmaceutical Quality GCP Auditor – Consulting

Posted 3 days ago

Apply now

About the role

  • GCP Audit role assessing compliance at clinical sites for Advarra. Collaborate with clients, prepare audit reports, and ensure quality standards for clinical trials.

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.
  • 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 German communication, verbal and written
  • Bachelor's degree

Benefits

  • Inclusive and collaborative environment
  • Opportunities for professional growth and development

Job title

Pharmaceutical Quality GCP Auditor – Consulting

Job type

Experience level

SeniorLead

Salary

Not specified

Degree requirement

Bachelor's Degree

Location requirements

Report this job

See something inaccurate? Let us know and we'll update the listing.

Report job