Validation Engineer Representative
: Job Details :

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). Essential duties and responsibilities:Generate, review, and execute documentation for commissioning, qualification, and validation studies (IQ, OQ, PQ) on equipment, facilities, and computerized systems ensuring compliance with cGMP. Support the validation schedule by collaborating with manufacturing, engineering, quality control (QC), and quality assurance (QA) teams for activities. Support the generation and execution of cleaning cycle development and validation activities, such as: sprayball coverage testing, reports, visual inspection...Validation Engineer, Validation, Representative, Support Engineer, Engineer, Technology