Supplier Quality Assurance - Sr. Associate
Supplier Quality Assurance - Sr. Associate
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Job Description
Use Your Power for Purpose
Every day Pfizers unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative always putting the patient first. Whether you are involved in development maintenance compliance or research analysis your contribution directly impacts patients.
This role supports the Pfizer Sanford NC Quality Operations department by performing Quality Assurance activities including supplier qualification and management enrollment of new materials and suppliers associated with clinical and/or commercial products and provides quality oversight of supplier incidents. In addition directly supports internal and external regulatory agency inspections.
What You Will Achieve
In this role you will:
- Perform QA assessments and approvals for supplier management Contributes to the interpretation of cGXPs for the commercial and clinical environment
- Able to resolve complex issues with minimal assistance from management Perform QA supplier management activities (supplier reassessments quality agreements audit reviews risk assessments compendial reviews)
- QA support and approval for qualification of new suppliers and materials
- QA support and approval of Supplier Corrective Action Requests (SCAR)
Shared Accountabilities:
- Support internal and external agency audits.
- Develops ability to train other team members on tasks.
- Identify and implement new processes and programs for quality and continuous improvement.
- Collaborates within the Pfizer network in support of Supplier Quality.
- Is capable of working outside the immediate subject area supporting a wider range of customers of differing subject areas and locations.
- Interacts with third party suppliers while maintaining Pfizer policies and values and ensures excellent customer service.
- Represents Quality Assurance in cross-departmental/cross-site/cross-network meetings/summits.
Here Is What You Need (Minimum Requirements)
- Bachelors Degree with at least 3 years of experience OR Masters Degree with more than 1 year of experience OR an Associates Degree with 6 years of experience OR a High School Diploma (or Equivalent) and 8 years of relevant experience .
- Solid understanding of current Good Manufacturing Practices and relevant GxP regulations and standards
- Strong critical thinking skills
- Ability to work effectively within own team and interdepartmental teams
Bonus Points If You Have (Preferred Requirements)
- Knowledge in cGXP materials components and supplier management
- Experience in quality administered systems
- Strong organizational skills and attention to detail
- Experience with regulatory compliance and documentation
- Ability to mentor and review the work of other colleagues
- SAP experience
NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS
- May require working non-standard hours or shifts
The annual base salary for this position ranges from $80300.00 to $133900.00. In addition this position is eligible for participation in Pfizers Global Performance Plan with a bonus target of 10.0% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of lifes moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution paid vacation holiday and personal days paid caregiver/parental and medical leave and health benefits to include medical prescription drug dental and vision coverage. Learn more at Pfizer Candidate Site U.S. Benefits (). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa FL or any location outside of the United States.
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 providers 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.
Required Experience:
Senior IC
Employment Type
Full-Time
