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QA Specialist IIIPfizer, S.A. de C.V • Andover, Minnesota, United States
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QA Specialist III

Pfizer, S.A. de C.V
  • US
    Andover, Minnesota, United States
  • US
    Andover, Minnesota, United States
Jetzt Bewerben

Über

Responsibilities
Evaluate and review clinical and commercial drug batches to ensure compliance with established specifications.
Conduct rigorous statistical process control procedures to identify deviations from standards.
Contribute to moderately complex projects, managing time effectively and developing short‑term work plans.
Investigate and document Quality Assurance deviations, escalating issues to the Quality Assurance Lead as needed.
Ensure regulatory compliance with current Good Manufacturing Practices (GxP) and provide Quality Review and oversight of site documentation to meet global regulatory and Pfizer quality standards.
Qualifications
Applicant must have a bachelor's degree with at least 2 years of experience; OR a master's degree with 0+ years of experience; OR an associate's 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.
Good working knowledge of Microsoft Excel and Word.
Proactive approach to problem‑solving.
Preferred Skills
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.
Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use.
Benefits and Compensation The annual base salary for this position ranges from $82,700.00 to $137,900.00. In addition, this position is eligible for participation in Pfizer’s 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 life’s moments. Benefits 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 such as medical, prescription drug, dental and vision coverage.
Work Location Hybrid. Relocation assistance may be available based on business needs and/or eligibility.
Employment 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.
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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  • Andover, Minnesota, United States

Sprachkenntnisse

  • English
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