Quick Info
Experience Level
Mid LevelMinimum Degree
BachelorDepartment
Quality Assurance ControlJob Type
Full TimeSpecialty 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).
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