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Quality Assurance Associate - GMP/Pharma QA
Job in
Cumberland, Providence County, Rhode Island, 02864, USA
Listed on 2026-10-06
Listing for:
Cedent
Full Time
position Listed on 2026-10-06
Job specializations:
-
Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist -
Pharmaceutical
Regulatory Compliance Specialist
Job Description & How to Apply Below
A pharmaceutical company in Cumberland, RI is seeking a Quality Assurance Associate I to ensure compliance with FDA and GMP regulations. The role involves providing QA oversight, conducting audits, and reviewing documentation. Candidates should have strong problem-solving and communication skills, as well as the ability to train staff in quality assurance best practices. This full-time position requires a commitment of 40 or more hours per week, and the opportunity offers a chance to improve quality systems in a critical industry.
Join us at Cedent as our next Quality Assurance Associate I - GMP/Pharma QA in Cumberland, RI, United States. The following position is for a Quality Assurance Associate I - GMP/Pharma QA with Cedent. Our group is growing, and we are hiring a Quality Assurance Associate I - GMP/Pharma QA in Cumberland, RI, United States.
Position Requirements
10+ Years
work experience
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