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