The Manager of Site Compliance is responsible for the Quality Systems within Lupin Somerset related to Internal Audits, Vendor Qualification and routine Annual Product Reviews. The Manager must have sufficient experience in evaluating pharmaceutical manufacturing practices and understand industry standards to appropriately evaluate practices and procedures and be very familiar with various types of manufacturing technologies and associated Quality Systems. The experience should include specific technologies such as wet granulation, fluid bed coating, high speed compression, encapsulation, tablet coating, and liquid filling. The qualified candidate has appropriate experience in dealing with Governmental officials within the FDA. Additional areas of responsibility include evaluating staffing needs, establishing requirements as per GMP and European standards, budget, training, prioritizing and scheduling of team activities and reporting quality progress on a monthly basis to site management. This position must assure all GMP systems are of the highest quality and meet all applicable standards.