Regulatory Affairs Specialist
GE HealthcareFull Time
Junior (1 to 2 years)
Key technologies and capabilities for this role
Common questions about this position
A Bachelor’s degree in Pharmaceutical Science or related field is required, along with a minimum of 1 year of experience in Regulatory Affairs for Cosmetics and Nutritional Products in Egypt or GCC. Experience with medical devices is a plus, plus strong knowledge of good documentation practices, proficiency in HA systems and Microsoft tools, and fluency in local language with good English command.
Responsibilities include preparing and reviewing regulatory documentation, supporting submissions through Health Authority systems, acting as a liaison between clients and regulatory bodies, identifying process improvements, and upholding quality standards.
This information is not specified in the job description.
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IQVIA offers continuous learning, career growth, and the chance to be part of a global team advancing healthcare through science and technology.
Advanced analytics and clinical research services
IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.