Jobs · Quality Assurance · Missouri

Director, Quality Management Systems/Validation & Compliance Lead

Pfizer · Chesterfield, MO · 1 wk ago
Quality Assurance$163k–$272k/yrFull-time

About the role

The QMS/V&C Lead is responsible for driving GWE R&D Compliance Program and Systems across Global sites. The incumbent will oversee, manage, and assure overall adherence to the Compliance Program for GWE R&D and drive GWE’s Continuous Improvement approach to service, customer and compliance assurance. The QMS/V&C Lead supports GWE R&D by driving strategy, compliance requirements, control, quality, and continuous improvements.

Responsibilities

  • Assures compliance for all site facility cGLP, cGCP, cGMP and other non-EHS compliance systems and activities
  • Budget responsibility for compliance functions
  • Oversees adherence to the GWE R&D document management strategy
  • Develops, manages, and reports progress to GWE R&D Leaders against the GWE Compliance Program and progress on implementation, gap closure, and strategy
  • Develops overall area program documentation and ensures documentation compliance
  • Plans, leads, and participates in management system audits, including the preparation of review report and identification of corrective actions and follow through
  • Verifies corrective action requests, monitors evaluation of responses, and determines if identified corrective action successfully resolves intent of findings/issues
  • Makes sure corrective actions are completed
  • Makes sure the GWE R&D area Compliance Program compliments existing PRD and ORD programs
  • Makes sure the Compliance Program is effective and identifies and implements changes based on efficiencies/changing business needs
  • Manages certification/registration efforts for the GWE R&D compliance
  • Facilitates GWE R&D SME team meetings in the development of short-term and long-term strategies and policies for applicable functional elements of the GWE R&D Compliance Program
  • Acts as the global point of contact for interpretation, maintenance, and continuous improvement of certain functional elements of the GWE R&D Compliance Program
  • Facilitates the development of annual GWE R&D compliance related objectives and goals
  • Conducts Site Risk Management Reviews and reports on the status and recommend areas of improvement to GWE R&D leadership
  • Provides guidance and feedback to site functional representatives regarding strategy, policy, and documentation activities
  • Facilitates the development of new approaches to solve site management system and business issues
  • Prepares comprehensive status reports and presentations for GWE R&D Site Leaders, GWE R&D Leader
  • Liaises with third party assessors in the site assessment of the department’s Quality Management System
  • Ensures appropriate correspondence with all internal and external area customers on any Management system-related matters

Qualifications

  • Bachelor’s Degree in relevant discipline and 8+ years of relevant work experience
  • Master's Degree in relevant discipline preferred

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