Senior Asset Quality Lead, Inspections (director)

Pfizer Com Sg

$176,600.00 to $294,300.00; bonus target of 20.0%;...
Gcp quality risk management
Inspection readiness strategy
Clinical development & operations quality
The Senior Asset Quality Lead, Inspections is responsible for driving GCP Quality by maintaining quality line-of-sight for assigned asset/franchise, bringing deep knowledge of GCP quality and risk management principles to asset and study teams

Job Summary

  • The Senior Asset Quality Lead, Inspections is responsible for driving GCP Quality by maintaining quality line-of-sight for assigned asset/franchise, bringing deep knowledge of GCP quality and risk management principles to asset and study teams.
  • This role will ensure asset and/or franchise quality oversight, drive quality risk management and inspection readiness activities, and be instrumental in ensuring that asset and study level information is appropriately incorporated within the GCP QMS.
  • The position offers a competitive salary range, eligibility for a Global Performance Plan with a bonus target, and participation in a share-based long-term incentive program, along with comprehensive benefits.

Matching Summary

The Senior Asset Quality Lead, Inspections is responsible for driving GCP Quality by maintaining quality line-of-sight for assigned asset/franchise, bringing deep knowledge of GCP quality and risk management principles to asset and study teams.

Salary

$176,600.00 to $294,300.00; Bonus target of 20.0%; Comprehensive and generous benefits

Skills & Requirements

Must-have

  • GCP Quality Risk Management
  • Inspection Readiness Strategy
  • Clinical Development & Operations Quality
  • Quality Oversight for Assets/Franchises
  • Business Development Due Diligence

Nice-to-have

  • Cross-functional leadership experience
  • Subject matter expert in Quality processes
  • Strong interpersonal skills
  • Ability to influence leaders

Key Requirements

  • 15+ years of relevant experience
  • BS – 10+ years or equivalent
  • MS/MBA – 9+ years or equivalent
  • Expert advanced knowledge in clinical trial development
  • Extensive knowledge of ICH GCP and regulations
  • Permanent work authorization in the United States

Work Rights

Permanent work authorization required

Tailored Resume

Cover Letter