Job description:Develop, review and approval of Validation Lifecycle Document, Validation Protocols and Reports including supporting discrepancies and deviations investigation / closure in line with RSTO policies and standards. Ensure that all validation activities with respect to equipment/facility qualification and cleaning validation stated in validation plan/ protocol are carried out in accordance with relevant policies, standards, procedures and guidelines, and completed in a timely fashion. Perform IQ, OQ and PQ of classified areas or equipment eg Biosafety cabinets, ISO 5 rooms. Comply with all RSTO’s Safety, Health & Environmental (SHE) requirements, never put oneself and others at safety & health risks, and report any workplace accidents, near misses and hazards as soon as practicable. Any other tasks as and when assigned by Supervisor. Engineering/Science Degree or higher from recognized institution Minimum 5 years of experience in Validation in the pharmaceutical/biotech industry or equivalent holders with combination of education and relative work experience Familiarity with Regulatory requirements and local Codes & Standards (e.g., FDA, EMEA, GAMP and ICHQ7). Good knowledge and experience of the practical and theoretical requirement of validation program in GMP facility Good oral and written communication skills Meticulous and Systematic Ability to adapt to rapidly changing priorities and the flexibility to support operations in accordance with the manufacturing schedule. Must be highly motivated, able to work independently as well as a Team player, with strong focus on safety, quality and timeline.