WHAT YOU WILL ACHIEVE
This position will support the Pfizer Sanford, NC Quality Assurance department by performing Quality Assurance activities related to supplier quality management associated with clinical and commercial product. Conducts programs designed to improve supplier performance, prepares/maintains quality assurance procedures to assure compliance with customer and/or government requirements. In addition, provides support for regulatory agency inspections, displays extensive knowledge of cGXP, functions as subject matter expert (SME) in supplier management, and provides leadership to other team members.
HOW YOU WILL ACHIEVE IT
Perform QA assessments and approvals for supplier management.
Interpretation of cGXPs for the commercial and clinical environment.
Able to resolve complex issues with minimal assistance from management.
QA supplier management activities (supplier reassessments, quality agreements, audit reviews, risk assessments).
QA support and approval for qualification of new suppliers and materials.
QA disposition of incoming materials, as applicable.
Organize and provide written and/or oral presentations of work with minimal input. Communicate status and provide performance metrics to the team and site management.
Ability to identify issues, present complex problems with possible solutions, and actively take leadership or independent role to resolve complex issues.
Provide guidance/coaching to less experienced colleagues.
Proactively promotes teamwork and motivates others to achieve team objectives.
Participate in external agency audits.
Trains other team members on tasks.
Identify and implement improvements to the supplier management process and other Quality Systems.
Interfaces with other parts of the organization such as Pfizer research and development groups. Able to work outside immediate subject area, supporting a wider range of customers of differing subject areas and locations.
Represents Quality Assurance in cross-departmental/cross-site/cross-network meetings/summits.
QUALIFICATIONS
Must-Have
Applicant must have a bachelor's degree with at least 5 years of experience; OR a master's degree with at least 3 years of experience; OR a PhD with 0+ years of experience; OR as associate's degree with 8 years of experience; OR a high school diploma (or equivalent) and 10 years of relevant experience.
Experience in manufacturing, quality or engineering in the biotech or pharmaceutical industry.
Strong communication and organization skills required.
Nice-to-Have
Prior experience working with Quality Assurance, supplier management, and/or Supply Chain preferred. Knowledge in cGXP, materials, components, and supplier management.
OTHER JOB DETAILS
Last Date to Apply for Job: November 6, 2025
Additional Location Information: NO
Eligible for Relocation Package – NO
Secondment 9 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 for 12 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.
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@pfizer.com. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.