Pharma Validation Engineer – cGMP Specialist
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Engineering
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Quality Assurance - QA/QC
Job Description & How to Apply Below
Actalent seeks a Validation Engineer for our Dallas, TX facility to manage qualification activities for manufacturing equipment, processes, and associated systems. You will lead IQ/OQ/PQ efforts, implement SPC monitoring, and ensure continued regulatory compliance within a cGMP environment.
This permanent, onsite role requires a BS in Engineering (Chemical preferred) and 3+ years of validation experience. Competitive hourly pay and comprehensive benefits are offered.
The Pharma Validation Engineer – cGMP Specialist position in the Engineering field is open for applications.
The Pharma Validation Engineer – cGMP Specialist role at ACTalent is now open for applications in Dallas, TX, United States.
Join us at ACTalent as our next Pharma Validation Engineer – cGMP Specialist in Dallas, TX, United States.
We are currently recruiting a Pharma Validation Engineer – cGMP Specialist for our team in Dallas, TX, United States.
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