Validation Supervisor

Responsibilities: A pharmaceutical company in Irvine is seeking a candidate for the position of Validation Supervisor. This individual will be supervising a staff comprised of 2 to 5 Validation Engineers (Levels I and II) and Technicians to support not only current validation/revalidation programs but also production, scientific affairs, and contract manufacturing operations with validated processes/equipment. Responsibilities & duties include: Supervise and coordinate activities of 2-5 Validation personnel. Provide technical support and guidance to other validation personnel or project team in protocol/report preparation, execution and data interpretation. Review validation protocols and use data analysis skills in assuring accurate interpretation of data. Track projects to ensure completion within defined time lines. Write, review, or revise SOPs as related to validation policies or revalidation activities, as needed. Independently prepare written validation protocols including designing appropriate test experiments. Assist the validation manager in providing technical assistance and handling any questions or concerns from contract customers or agencies in reference to validation activities. Follow Safety, Health, and Environmental policies and procedures. Perform other duties, as assigned, or as business needs require.If you are not a local candidate but are relocating, please inform me of your arrangements (i.e., date and city/state you are relocating to).Kforce (NASDAQ: KFRC) is a full-service specialty staffing firm providing flexible and permanent staffing solutions for organizations and career management for individuals in the specialty skill areas of information technology, finance & accounting, human resources, engineering, pharmaceutical, health care and scientific. Backed by more than 1,500 recruiting specialists, Kforce operates in more than 40 markets in North America. For more information, please visit our web site at