Pharma Validation Specialist: IQ/OQ/PQ, GMP, CSV Expert
Listed on 2026-09-30
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering -
Pharmaceutical
Regulatory Compliance Specialist, Pharma Engineer, Quality Engineering, Pharmaceutical Manufacturing
Akaasa Technologies is seeking a hands-on pharmaceutical validation professional to support equipment, utilities and process validation within GMP systems. You will execute IQ/OQ/PQ protocols, manage deviations, and drive CAPAs while maintaining data integrity across validated systems.
The ideal candidate has 3+ years in pharma validation, strong regulatory knowledge (FDA/EMA/ICH/GAMP5), and collaborates with QA, QC, engineering, and manufacturing teams to ensure compliant, reliable operations.
The Pharma Validation Specialist: IQ/OQ/PQ, GMP, CSV Expert role at Akaasa Technologies is now open for applications in NC, United States.
Learn more about the Pharma Validation Specialist: IQ/OQ/PQ, GMP, CSV Expert role in the description above.
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