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Associate Director GCP Quality Assurance
Associate Director GCP Quality AssuranceMeet Life Sciences • San Francisco, CA, United States
Associate Director GCP Quality Assurance

Associate Director GCP Quality Assurance

Meet Life Sciences • San Francisco, CA, United States
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Associate Director GCP Quality Assurance

Base pay range

$180,000.00 / yr - $210,000.00 / yr

Associate Director, GCP Quality Assurance

Location : SF Bay Area – 5 days onsite

Overview

The Associate Director, GCP QA plays a key role in driving consistency across Quality systems and processes supporting Clinical programs. This role partners closely with GCP QA and Clinical Operations Quality Management to support day-to-day clinical trial activities, including deviations, investigations, audit findings, and CAPA management. The position also contributes to inspection readiness efforts and provides cross-functional guidance on compliance and quality expectations.

Key Responsibilities

  • Lead alignment and oversight of Quality Systems across Clinical QA.
  • Assess current processes, identify gaps, implement improvements, and monitor GCP-related Quality Systems.
  • Develop and manage reports tracking key GCP and Clinical Quality metrics.
  • Review and approve deviations and CAPAs.
  • Partner with Regulatory, Clinical Operations, and other stakeholders on compliance issues.
  • Maintain up-to-date knowledge of Health Authority regulations and advise Clinical teams on impacts.
  • Represent Clinical QA in internal presentations and quality initiatives.
  • Identify and escape risks, proposing practical solutions.
  • Contribute to process and system improvement activities.

Education & Experience

  • Bachelor’s degree with ~11+ years of relevant experience,
  • or Master’s with ~9+ years,
  • or PhD with ~5+ years,
  • or an equivalent combination of education and experience.
  • Minimum 10 years of experience in pharma / biotech.
  • Strong background in GCP and Quality Systems, including continuous improvement and Quality Risk Management.
  • Deep understanding of clinical trial processes and GCP QA oversight.
  • Ability to analyze complex quality issues and apply risk-based approaches.
  • Experience developing metrics and contributing to quality strategy.
  • Strong collaboration, influencing, and communication skills.
  • Seniority level

    Director

    Employment type

    Full-time

    Job function

    Quality Assurance

    Industries

    Staffing and Recruiting, Pharmaceutical Manufacturing, and Biotechnology Research

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