QC Scientist

Company Overview

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver meets the highest standards of safety and efficacy.

• Investigate and write or review Laboratory Investigations and/or Non-Conformance Deviations.
• Support the Quality Control Organization by supporting trending, department-wide initiatives, investigation training, and continuous improvement activities.
• Maintain compliance with Current Good Manufacturing Practices in Quality Control laboratories.
• Utilize Laboratory Information Management System and other data systems as warranted.
• Serve on cross-functional teams, participate in audits, conduct safety inspections, recommend corrective actions, and train junior colleagues.

• Bachelor's degree with at least 2 years of experience, OR Master's degree with 0+ years of experience, OR Associate's degree with 6 years of experience, OR High school diploma (or equivalent) with 8 years of relevant experience.
• Strong problem-solving abilities.
• Understanding of pharmaceutical manufacturing, Quality Control testing, packaging, and quality assurance operations.
• Detail-oriented with robust knowledge of quality systems.
• Ability to receive feedback and take accountability for actions and personal development.
• Strong project management skills.
• Effective written and verbal communication, as well as interpersonal skills.

• Relevant pharmaceutical experience.
• Strong understanding of computer system hardware, infrastructure, and networks.
• Experience with Laboratory Information Management Systems (LIMS).
• Proficiency in data analysis and interpretation.
• Knowledge of regulatory requirements and guidelines.
• Laboratory experience.
• Effective time management and organizational skills.
• Ability to mentor and train junior 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.

Normal lifting, sitting, standing and walking requirements to facilitate support of staff in the office and on the floor (laboratory, suites, etc.).

Position is first shift Monday through Friday. Some off hour (night/weekend/holiday) support may be required.

Last Date to Apply:
June 26, 2026. Referral Bonus Eligibility: YES. Relocation Package: NO. Work Location Assignment:
Hybrid. The annual base salary ranges from $82,700.00 to $. Eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 10.0% of the base salary.

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 to include medical, prescription drug, dental and vision coverage.

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.