GMP Investigations Associate — Quality & Compliance
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Quality Assurance - QA/QC
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Manufacturing / Production
Job Description & How to Apply Below
Pfizer seeks a GMP investigator to lead manufacturing deviation investigations within its quality systems. You will coordinate data collection from manufacturing, laboratory data and audit trails to determine root causes and drive CAPAs with cross‑functional teams.
The role requires strong technical writing skills, familiarity with GMP records, and experience in biotech manufacturing or lab settings. On‑premise location and competitive benefits apply.
As a GMP Investigations Associate — Quality & Compliance, you will play an important part at Pfizer in Andover, MA, United States.
This role, GMP Investigations Associate — Quality & Compliance at Pfizer, could be your next move.
Are you ready to take on the GMP Investigations Associate — Quality & Compliance role at Pfizer?
We would love to welcome a new GMP Investigations Associate — Quality & Compliance to our group in Andover, MA, United States.
Position Requirements
10+ Years work experience(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
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