• 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