GMP Investigations Associate — Quality & Compliance

Pfizer; Andover (MA); On-site; USD 60,000 - 100,000; Full time

Benefits offered by this job

401(k) with matching

Paid vacation & holidays

Health benefits

Job summary

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.

Qualifications

• Bachelor’s degree with 0–2 years, or an Associate’s with 4 years, or HS diploma with 6 years relevant experience.
• Strong technical writing and documentation skills with ability to author GMP records.
• Experience in GMP biotech manufacturing or lab environment.

Responsibilities

• Lead and author GMP investigations within Pfizer quality systems.
• Coordinate cross‑functional investigation teams and determine root causes.
• Define corrective and preventive actions and ensure timely completion.

Skills

Technical writing

Data analysis

Quality systems

Education

Bachelor's degree

Associate's degree

Tools

DeltaV

SAP

LIMS

Electronic batch records

Job description

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.