Regulatory Affairs Graduate Intern - Tamheer Program

Assist in preparing and submitting regulatory submissions Support updates to Technical Documentation to align with EU Medical Device Regulation (MDR) Help improve regulatory processes, including database maintenance, automation, and regulatory controls Work with different departments to ensure compliance Conduct data collection, analysis, and interpretation to support regulatory decisions Pursuing a degree in Science or Healthcare-related fields, such as Engineering, Legal, Communication, Master's degree in Regulatory, Clinical Affairs, or Public Health Skills & Experience Excellent written and verbal communication skills. Basic understanding of data collection, analysis, and interpretation Strong computer skills, including word processing, PowerPoint, and database management. Ability to translate technical information into clear documentation. Quick learner, self-motivated, and able to work independently. TAMHEER eligibility. TAQAT registration for TAMHEER. No prior TAMHEER participation. Not registered in GOSI for the past 6 months. Immediate availability to start. Understanding of clinical data. Understanding of health economics data advantageous. Excellent communications skills, written and oral in English. Good computer skills (e.g. Excel spreadsheets, PowerPoint presentation and MS Office applications).