Two to four (2-4) years of experience working within the biotherapeutic and/or pharmaceutical industry and knowledge in compliance of commissioning, qualification and validation of GMP processes and systems such as Utilities (water for injection, clean steam, process gases, HVAC, SIP/CIP), fridges, freezers, LAF, BSC units, autoclaves and isolators as well as Process Equipment Bioreactors, UF/DF, centrifuge, Chromatography systems. This position is responsible for ensuring compliance with regulatory requirements and company policies following current Good Manufacturing Practices, client's Policies and internal procedures through the following duties and responsibilities: " Ensure the site validation program has been developed and maintained in compliance with all regulatory and corporate requirements and Master Plans.