Site Quality Systems Lead (Secondment 12 Months)

WHY PATIENTS NEED YOU

The QO Systems Lead is responsible for the operational and strategic management of Quality Systems. The QO Systems Lead ensures that the Validation Change Control Training Documentation Applications and Human Performance programs comply with cGMP standards and corporate quality standards while partnering with site management team to effectively design develop and implement processes to support business goals and site strategies. This position will be a member of the site Quality Leadership team (QLT) and will report to the Site Quality Operations Leader (SQOL).

WHAT YOU WILL ACHIEVE

• Provide operational and strategic leadership to QO Systems teams to define goals & objectives and drive performance.

• Ensuring adherence to applicable regulations and Pfizer Quality Standards.

• Ensuring the Quality system requirements are effectively established and monitored.

• Build Quality into the product transfers to ensure high quality product is consistently manufactured and tested per validated processes.

• Holds self and the team accountable for making decisions deriving solutions or driving improvements for the areas in scope.

• Partner with stakeholders to improve and sustain metrics through continuous improvement.

• People development coach and mentor team to demonstrate excellence. Build the culture of active learning inculcating the Pfizer value of Joy.

• Represents the site Quality Systems team in limited duration teams cross-departmental/cross-site/cross-network meetings as needed and able to carry out activities as requested by the Site Quality Operations Leader.

• Responsible for role modeling coaching and ensuring others embody Pfizer values and behaviors.

QUALIFICATIONS

Must-Have

• Applicant must have a bachelors degree with at least 8 years ofexperience; OR a masters degree withat least 7 years of experience; ORa PhD with 5 years of experience.

• Manufacturing quality or engineering experience in the biotech or pharmaceutical industry with a BS Degree in Sciences or Engineering.

• Previous leadership experience required and experience in leading people leaders and directing organizations.

• Knowledge and experience in Quality Systems Deviations Change controls CAPA Validation Change Control Training & Documentation control.

• 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.

Nice-to-Have

• Experience supporting Board of Health inspections.

OTHER JOB DETAILS

• Last Date to Apply for Job:April 13 2026

• Additional Location Information:NA

• Eligible for Relocation Package NO

• Secondment12 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.

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.