Associate Director, Global Quality Compliance Lead at Teva Pharmaceuticals - ScoutJobs - The AI-curated global job board
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Teva Pharmaceuticals
Posted 13 hours ago

Associate Director, Global Quality Compliance Lead

Teva Pharmaceuticals

Requirements

Bachelor's degree, 8-12 years pharmaceutical quality/compliance experience, GMP-regulated manufacturing experience, Sterile manufacturing expertise, Health Authority inspection support experience, Microbiology quality systems knowledge

Skills

GMPMicrobiology

About the role

Responsibilities

  • Lead global quality compliance initiatives and projects focused on patient supply, quality systems improvement, and deviation reduction.
  • Support inspection readiness and Health Authority inspections (FDA, EMA, MHRA, etc.), including SME preparation, coaching, and remediation.
  • Provide sterility assurance and contamination control expertise, including oversight of contamination control strategies (CCS) and environmental monitoring.
  • Oversee product quality incident management and lead complex investigations using robust root cause analysis and CAPA processes.
  • Develop and monitor Quality Improvement Plans (QIPs) and KPI performance measures to minimize compliance risk.
  • Partner cross-functionally on global safety labeling programs and Pharmacovigilance inspection readiness.
  • Represent the company in industry working groups and contribute to regulatory policy discussions.

Requirements

  • Bachelor’s degree in a related field (higher education preferred).
  • 8-12 years of pharmaceutical quality or compliance experience in GMP-regulated manufacturing environments.
  • Strong expertise in sterile manufacturing, biologics, or medical devices.
  • Direct experience supporting Health Authority inspections and managing inspection responses.
  • Hands-on experience with microbiology quality systems, including sterility testing, bioburden, and endotoxin testing.
  • Proven ability to manage cross-site or global quality compliance initiatives.
  • Ability to travel up to 30% domestically and internationally.

Preferred Qualifications

  • Advanced knowledge of cGMPs, quality systems, audits, and risk management.
  • Experience with Veeva implementation and modernization initiatives.
  • Strong leadership and project management skills within a highly matrixed global environment.

Benefits

  • Generous annual leave and flexible working schedules.
  • Access to tailored health support and reward plans.
  • Professional development opportunities through the Twist career platform.
  • Meaningful ways to give back to the community.

About the Company

Teva is a leading innovative biopharmaceutical company dedicated to addressing patients' needs through neuroscience, immunology, and high-quality generic medicines worldwide. We foster a high-performing, inclusive culture that values collaboration and fresh thinking.

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Associate Director, Global Quality Compliance Lead

Teva Pharmaceuticals · Waterford

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