Quality Assurance Associate III
PfizerAbout the role
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 is of the highest standard. Your role is crucial in maintaining this commitment and driving forward our mission to improve patient outcomes.
What You Will Achieve
In this role, you will:
Perform activities within the North Creek Compliance group with a focus on Supplier Change Notifications.
Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Contributes to the completion of specific programs and projects.
Demonstrates good judgment in selecting methods and techniques for obtaining solutions. Uses ability as a Quality Professional in accordance with company policies and procedures to complete complex tasks in creative and effective ways.
Normally receives limited instruction on day-to-day work, general instructions on new assignments.
Independently determines and develops approach to solutions.
Be an individual contributor with no people management responsibilities.
How you will achive it
Work with corporate SQM and Site functional areas to review, assess and document impact to North Creek from Supplier Change Notifications.
Compliance with approved procedures and cGMP expectations. Communicate and resolve discrepancies with external and internal partners
Coordinate cross functional meetings to assess Supplier Change Notifications and document functional Area assessment.
Work With external customers to obtain change notifications and required information to enable a comprehensive review.
Act as the Responsible person for Deviations and Change Controls for associated Supplier Change Notifications.
Work with other Compliance areas to implement corrective actions/mitigation strategies for impacted materials.
Write and review Standard Operating Procedures as needed
Support other Compliance activities as needed.
Proficiency with electronic Quality Management Systems (QMS), electronic documentation management systems (eDMS) and inventory management systems (SAP).
Here Is What You Need (Minimum Requirements)
Bachelor's degree in a scientific discipline with any years of experience, or an Associate's degree with 4 years of relevant experience, or a high school diploma (or equivalent) and 6 years of relevant experience
Industry experience in a cGMP/FDA regulated environment such as Manufacturing, QC or QA
Detail oriented team player with effective planning, organization, and execution skills
Excellent communication skills with internal and external personnel essential
Ability to work effectively at a fast pace with cross functional departments
Experience with quality management systems (QMS), electronic documentation management systems (eDMS) and inventory management systems (SAP)
Bonus Points If You Have (Preferred Requirements)
Experience with plant operations, pharmaceutical/biotechnology manufacturing and Quality Control analytical testing.
Strong problem-solving skills
Ability to work independently and as part of a team
Excellent time management and multitasking abilities
Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance
Other job details
Last day to apply: April 27th, 2026
Work Location Assignment: Hybrid
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