Senior Asset Quality Lead, Inspections (director)

pfizer.de

Base: $176,600.00 to $294,300.00; bonus/equity: 20...
Gcp quality and risk management
Inspection readiness and support
Clinical trial quality oversight
The Senior Asset Quality Lead is responsible for driving GCP Quality by maintaining quality line-of-sight for assigned assets and franchises and ensuring inspection readiness activities

Job Summary

  • The Senior Asset Quality Lead is responsible for driving GCP Quality by maintaining quality line-of-sight for assigned assets and franchises and ensuring inspection readiness activities.
  • This role partners with cross-functional teams to provide quality risk management, quality issues management, and serves as a subject matter expert within Clinical Development & Operations Quality.
  • Pfizer offers a competitive salary range, bonus opportunities, share-based long term incentives, and comprehensive benefits including retirement plans, paid leave, and health coverage.

Matching Summary

The Senior Asset Quality Lead is responsible for driving GCP Quality by maintaining quality line-of-sight for assigned assets and franchises and ensuring inspection readiness activities.

Salary

Base: $176,600.00 to $294,300.00; Bonus/Equity: 20% bonus target and share-based long term incentives; Benefits: 401(k) with matching, paid leave, health coverage

Skills & Requirements

Must-have

  • GCP quality and risk management
  • Inspection readiness and support
  • Clinical trial quality oversight
  • Quality risk planning and escalation
  • Quality integration for business deals
  • Quality metrics and compliance management

Nice-to-have

  • Cross-functional leadership experience
  • Strong interpersonal and influencing skills
  • Experience leading global initiatives
  • Knowledge of Pfizer processes and SOPs
  • Therapeutic area familiarity
  • Training and mentoring capabilities

Key Requirements

  • Preferred 15+ years relevant experience
  • BS degree with 10+ years experience or MS/MBA with 9+ years
  • Expert knowledge of ICH GCP and regulations
  • Experience in clinical trial operational quality management
  • Permanent US work authorization required

Work Rights

Permanent US work authorization required

Tailored Resume

Cover Letter