Pharma Validation Specialist: IQ/OQ/PQ, GMP, CSV Expert
Listed on 2026-09-28
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering -
Pharmaceutical
Regulatory Compliance Specialist, Pharma Engineer, Quality Engineering
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.
Consider building your career as a Pharma Validation Specialist: IQ/OQ/PQ, GMP, CSV Expert at Akaasa Technologies.
The position is based in NC, United States.
This opportunity is part of our work in Engineering.
The advertised compensation is 90..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
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