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Job Description

• Good knowledge about writing SOP, validation protocols and other related documents in Technical department • Familiar with international GMP guidelines specially PIC/S • Organizing and execution of IQ, OQ and PQ protocols • Planning and execution of FAT and SAT protocols • Technical Team Management • PM management for all utilities and facilities • Coordination with Project Manager for OSD Manufacturing Site

Requirements

• University Qualifications: MS or higher related engineering degrees • Preferably at least 3-5 years direct and related experience in pharmaceutical industry • Experience in qualification and validation of utilities (HVAC) and process instruments • Familiar with Facilities, Utilities and processing machineries in OSD pharmaceutical manufacturer. • familiar with ISPE requirements. • Ability to work in a team environment, handle multiple tasks • Being able to handle the stress of tight deadlines and a fast paced work environment • A strong knowledge of MS office programs. • Excellent documentation skills • Flexibility and adaptability • Excellent command of English

Employment Type