Manager, Vendor Operations Quality (Secondment 12-18 Months)

Why Patients Need You

Every day our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible innovative and customer-oriented culture is rooted in science and risk-based compliance. Whether you are involved in development maintenance compliance or analysis through research programs your contribution directly impacts patients. This is a global quality position within Vendor Operations Quality reporting to Vendor Operations Lead.

What You Will Achieve

This role is responsible for the quality system oversight of outsourced manufacturing and analytical operations for API drug substance drug product clinical supplies in support of Biologics (BTx) and Small Molecule (PSSM) portfolios including vaccines and Hospital Business products and new manufacturing technologies under development by PharmSci. An essential component of this role is to be able to work cross functionally in a matrix environment drive continuous improvement and influence both internal and external stakeholders.

How You Will Achieve It

In this role you will:

• Lead and guide moderately complex projects managing time and resources effectively and apply skills and discipline knowledge to departmental work

• Make decisions to resolve moderately complex problems develop new options guided by policies and operate independently in ambiguous situations

• Utilize judgment and experience to potentially become a resource for others and evaluate clinical and commercial drug batches to ensure adherence to specifications

• Identify deviations in manufacturing and packaging processes approve investigations and change control activities and guide operational teams in project management

• Prepare forecasts for resource requirements identify areas for improvement and facilitate agreements between different teams using leadership skills

• Lead continuous inspection readiness and drive effective management of quality issues and CAPAs

• Participate in internal cGMP audits support regulatory inspections perform disposition of clinical trial materials and communicate with internal and external customers to resolve project-related issues

• Ensure effective internal networking to develop and maintain business partner relationships with internal colleagues

• Utilize Pfizer systems such as SharePoint Supplier Management System Global Document Management System Clementine eQMS and Spotfire to manage daily work

• Manage lifecycle of vendor including qualification quality agreement performance monitoring quality site visits

Qualifications

Must-Have

• Applicant must have a bachelors degree with at least 5 years ofexperience; OR a masters degree with at least 3 years of experience; ORa PhD with 0 years of experience; OR as associates degree with 8 yearsof experience; OR a high school diploma (or equivalent) and 10 years ofrelevant experience.

• Substantial experience in pharmaceutical manufacturing and quality control

• Familiarity with Current Good Manufacturing Practices (cGMP) and handling compliance issues arising from cGMP deviations

• Knowledge of regulations related to vendor management programs and other industry quality systems

• Strong critical thinking skills and a proactive approach

• Ability to collaborate effectively manage relationships and communicate well both in writing and verbally

• Advanced computer skills in MS Office applications and a good understanding of enterprise systems such as eQMS SMS GDMS

Nice-to-Have

• Knowledge or exposure to data science

• Strong leadership and team management skills

• Ability to work under pressure and meet tight deadlines

• Ability to influence and negotiate with stakeholders

• Experience in conducting internal audits and supporting regulatory inspections

PHYSICAL/MENTAL REQUIREMENTS

Mental agility to handle strategic decision-making across different divisions of the organization (i.e. in collaboration with Quality Site leaders across the network Portfolio Leads including above site leaders)

NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS

<10% travel may be required

Ability to flex work schedule when required to meet the needs of the global organization

Other Job Details

• Last Date to Apply for Job:September 19 2025

• Additional Location Information:UK - Sandwich MA - Andover MO - St. Louis - Chesterfield

• Eligible for Relocation Package NO

• Secondment 12-18 months

• If you are currently in a driving position with a fleet vehicle and this secondment does not require driving as an essential function of the position for12 months or longer you will be required to turn in your fleet vehicle for the duration of the non-driving secondment. Please refer to the Fleet Policy and Procedures document for more information.

• There will be no change to your current work location.

• Position is considered Flexible and colleagues are expected to comply with Log In For Your Day(LIFYD) requirements at site location (e.g. about 2.5 days a week in office).

• Note: This secondment offers a valuable opportunity for professional growth. It will need to be funded by the secondees home market.

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