Director, Quality Management SystemsValidation & Compliance Lead

ROLE SUMMARY

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 GWEs 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 the Compliance area the Director provides strategy management advice ownership and guidance to all applicable GWE R&D functions by identifying short-term and long-term strategy daily interpretation and application of compliance requirements for services managed by GWE R&D. In addition the Director is responsible for assuring compliance with corporate policies for GWE R&D. Lead the design deployment training and subsequent continuous improvement of applicable global functional elements of the Compliance Program. Be responsible to direct the management of compliance functions (e.g. validation documentation and training) in support of cGLPs cGCPs cGMPs as well as other non-EHS regulatory regulations. The position will work in conjunction with GWE colleagues contractors R&D business units R&D research units and vendor resources to manage initiatives and assure regulatory compliance.

ROLE RESPONSIBILITIES

The major duties and responsibilities for QMS/V&C will include but are not limited to:

• 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
• Monitors and drives completion of quality review corrective actions
• Engages site stakeholders including GWE colleagues strategic partners vendors and customers and other resources in the development of the area Compliance program
• Ensures the consistent application of and adherence to the Compliance Program across all GWE R&D area functions
• Ensures the GWE R&D area Compliance Program compliments existing PRD and ORD programs
• Monitors the overall Compliance Program effectiveness and identifies and implements changes based on efficiencies/changing business needs
• Identifies and leads area 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
• Global contact for interpretation maintenance and continuous improvement of certain functional elements of the GWE R&D Compliance Program
• Global point of contact for interpretation of all functional elements of the GWE R&D Compliance Program
• Facilitates 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
• Issues maintains and controls all site-level compliance system procedures and related documents
• 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 departments Quality Management System
• Ensures appropriate correspondence with all internal and external area customers on any Management system-related matters.

BASIC QUALIFICATIONS

• Bachelors Degree in relevant discipline and 8 years of relevant work experience.

PREFERRED QUALIFICATIONS

• Masters Degree in relevant discipline
• 15 years experience in facility management engineering or compliance related area of pharmaceutical business
• First class interpersonal skills required to develop effective relationships at all levels throughout the business
• Proven financial management and analytical skills to ensure the cost-effective provision of business services across Pfizer
• Able to translate customer needs into action and meet needs of customer
• Able to ensure business continuity and develop appropriate business contingencies
• Able to create and implement strategy in own work area
• Able to create an environment in which Pfizer core values are valued through leading by example in these values
• Can advise and influence senior management and colleagues to ensure high performance
• Responsible for developing and training of staff in own work area to maintain best caliber individuals

MINIMUM KNOWLEDGE:

• Detailed understanding of Facilities Management marketplace particularly delivery of hard and soft services
• Proven financial management experience
• Have track record of sustaining effective relationships with customers and external and internal service providers
• Proven experience of bottom line focus and able to implement in own work area to demonstrate costs savings and efficiencies
• Track record with experience at senior level
• Able to demonstrate a professional career and subject matter expertise within Facility Management and Quality Management Systems
• Experience of managing multi-disciplinary teams
• Need to demonstrate the ability to perform a highly professional role
• Ability to develop services and implement new policies and strategies
• Proven knowledge/prior experience implementing and managing and maintaining quality systems (e.g. ISO 9000 Malcolm Baldrige etc.); technical records and six sigma experience a plus
• Demonstrated thorough understanding of GLPs GCPs and GMPs
• High level of leadership capability and credibility and ability to influence
• Skilled at team facilitation to build consensus and reach decisions
• Strong effective and proactive communicator particularly across global sites and customers
• Knowledge of GWE business functions and/or pharmaceutical R&D line knowledge

Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers develop and coach others oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.

PHYSICAL/MENTAL REQUIREMENTS

Due to the nature of work assignments incumbents must be able to perform detailed work on multiple concurrent tasks with frequent interruptions and under time constraints. On a daily basis the position responsibilities may require the ability to stoop; to reach; to stand to walk the site for extended periods of time; to push and/or pull objects weighing up to 30 pounds; to lift and carry objects weighing up to 15 pounds; to use finger dexterity to operate a computer and other office equipment and hand strength to grasp objects; to perceive the attributes of objects by touch; to hear and verbally exchange ideas and information with colleagues and others on the phone and in the office; to see clearly from less than one foot to arms length with a good field of vision and to distinguish basic colors and shades of color. On a frequent basis essential duties of the position may require the ability to climb stairs to kneel and/or crouch to retrieve items.

NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS

Day shift with occasional after hours or weekend response required

Periodic travel may be required in support of GWE business needs

Respond to the site in support of business continuity emergency response and off-shift schedules periodically

Entry and work in laboratory spaces GxP aseptic space mechanical/electrical rooms Central Utility Plant services areas such as maintenance shops shipping and receiving service corridors with adherence to personal protective equipment practices and procedures as well as aseptic gowning and procedures.

Work Location Assignment:Hybrid

Last Date to Apply for Job: 7/20/2026

Relocation assistance may be available based on business needs and/or eligibility.

Candidates must be authorized to be employed in the U.S. by any employer.

U.S. work visa sponsorship (such as TN O-1 H-1B etc.) is not available for this role now or in the future.

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