Requirements

• Good knowledge about writing SOP and other related documents • Familiar with international GMP guidelines specially PIC/S • Familiar with Pharmacopeia especially USP • Proven track record in regulatory affairs with strong connection to health care authorities. • Preferably reputable with credibility in font of MOH • 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. • Strong communication skills • Excellent documentation skills • Flexibility and adaptability • Excellent command of English