Every day everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture rooted in science and risk-based compliance is both flexible and innovative always putting the customer first. Whether your role involves development maintenance compliance or research analysis your contributions are vital and directly impact patients. Our dedication to quality and safety ensures that we consistently meet the highest standards making a real difference in the lives of those we serve. As the site Quality Risk management Lead at Sanford you will drive compliance and performance excellence. The role will provide oversight of the application of the Quality Risk management program technical expertise as well as drive compliance initiatives support inspection readiness and continuous improvement projects. This position will work closely with other site operating units as well as site leadership and the above site QRM team.
In this role you will:
Leads the integration of Quality Risk Management (QRM) principles and practices into the Quality System Develops QRM Plan for site
Ensures all aspects of the Quality Risk Management lifecycle and program are in place and properly functioning
Manages the deployment of site risk facilitators and QRM training
Participates in PCT meetings within network
Supports risk management during audits/inspections
Reports site QRM metrics
Ensures deployment of Risk Register and QRM Maturity Assessment
Provide technical inputs to evaluate QRM activities and accountable to provide leadership to drive issues to timely resolution.
Lead successful and timely execution of quality and compliance improvement initiatives.
Drive compliance excellence by ensuring GMP inspection readiness for Regulatory Authorities and site inspection readiness.
Applicant must have a Bachelors degree with at least 4 years of experience OR Masters degree with more than 2 years of experience OR a PhD with 0 years of experience OR an Associates degree with 8 years of experience OR High School Diploma (or Equivalent) and 10 years of relevant experience.
Experience in Quality Risk Management
Previous experience with leading projects is required.
The candidate must have excellent verbal and written communication skills with the ability to share vision direction and data with colleagues across all levels and in a wide range of different work groups.
The candidate must have demonstrated proficiency in organizational and project management skills and must be able to balance multiple priorities.
Experience interfacing with regulators/inspectors
Ability to communicate effectively across diverse functional groups and layers of management.
Strong Technical writing skills
Able to collaborate and partner cross-functionally
In depth knowledge and understanding of GMP regulations and Quality System requirements
Last day to apply: January 20th 2026
Work Location Assignment:On Premise
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
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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.
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Required Experience:
Manager
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