A

Validation Engineer

Agilent

📍 Frederick, CO

Posted 3 months ago

Quick Info

Experience Level

Mid Level

Minimum Degree

Bachelor

Department

Quality Assurance Control
0

Job Type

Full Time

Specialty Skills

Cleaning ValidationEquipment CommissioningEquipment ValidationAPI ManufacturingGMP

About the Role

Performs cleaning validation and equipment commissioning and validation engineering duties to support initial start-up and qualification of a new Active Pharmaceutical Ingredient (API) manufacturing facility at Agilent Technologies Nucleic Acid Solutions Division in Frederick, Colorado. Primary responsibilities include the execution, reporting, and communication of validation activities compliant with pharmaceutical Good Manufacturing Practices (GMP).

About Agilent

High-Throughput Screening Equipment, Imaging instruments

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