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Validation Specialist -WYETH-USA- Fort Dodge, IA
The primary functions of the Validation Specialist are to provide appropriate validation documentation for validation activities at the Fort Dodge facility, track and facilitate the completion of those activities, perform and/or assist with protocol execution, and provide adequate training within the Technical Services department.
RESPONSIBILITIES:
• Develop assigned protocols, reports and Validation Master Plans for the Parenteral production facility.
• Supervise assigned validation activities for the Parenteral production facility and interact as part of the focus factory team supporting that area..
• Review validation documentation for cGMP compliance.
• Interface with regulatory inspectors (supervised).
• Assist with the completion of assignments to meet major department objectives.
• Perform duties as assigned by the Manager(s) or Associate Director of Technical Services.
