Scientist - Regulatory Affairs

Job Location DUBAI GENERAL OFFICE Job Description Overview of the job In this role, you will be a key driver behind our continued growth and success. With our commitment to innovation, you will seek out, develop, and help implement strategic initiatives for improved efficiency and productivity. From creating regulatory affairs strategies to executing product submissions and registrations across the Middle East and Africa, you need to be a detailed planner, excellent communicator, and expert in regulatory affairs. You will be dedicated to ensuring regulatory compliance and facilitating market access for our products, navigating complex regulatory landscapes with precision and expertise. Your team This role reports to Senior Manager Regulatory Affairs Middle East & Africa & will look after Middle East & Africa countries. How Success Looks Like • You understand regulatory requirements deeply and apply them effectively to ensure compliance across the Middle East and Africa markets. • You execute and implement regulatory strategies that streamline product submissions and registrations, resulting in timely market access and minimal delays. • You provide strategic guidance and support to cross-functional teams, ensuring regulatory considerations are integrated into product development and business processes. • You proactively identify potential regulatory risks and develop strategies to ensure continuous compliance and business continuity. • You effectively foster a culture of excellence, collaboration, and professional growth within the regulatory affairs function and the company Responsibilities of the role • Work autonomously, but in alignment with local manager, to coordinate day-to-day Regulatory Affairs activities for specific area(s) of responsibility. • Understands the regulatory landscape across Middle East , Monitors the regulatory environment and provides assessments of the impact of new and changing regulations on the company's areas of interest. • Handles compliance within the department by ensuring global, regional, and local processes, policies, SOPs and working instructions are in place and adhered to. • Handles the coordination, compilation and submission of regulatory submissions, responses to regulatory agencies questions and other correspondence in accordance with regulatory agency regulations and guidelines and the country specific requirements. • Works with substantial discretion and uses best practices and knowledge of internal or external business issues to improve products or services. • Uses specialist knowledge, analytical skills, judgment, and broad conceptual and practical experience to solve complex problems and to contribute to process improvements. • Understands how the different teams jointly achieve the objectives of the area and uses knowledge of the organization, processes, customers, and key business drivers to increase effectiveness. Core Regulatory Practices: • To prepare & submit registration dossiers and to achieve registration for the specific product portfolio, within agreed timelines. • To update and maintain dossiers post registration, to ensure compliance with corporate and health authority legal requirements. This will include the submission of variation documents. • To ensure the renewal of registration of products by defining the accurate timelines. • To ensure maintenance and update of regulatory files and records including appropriate archiving of all relevant documentation in appropriate system in line with applicable internal company standards • To review and ensure the conformity of the product artworks, promotional material and tools with the marketing code and legal requirements. • To Liaise with health authorities, distributors, regulatory authorities to achieve and maintain registrations. • Leads, monitors, assesses, and communicates risks on key projects, providing regular updates to Stakeholders and Management • Monitors and progress of applications against set timelines, acting where necessary, to minimize delays and anticipate difficulties/challenges. • Communicates information and presents status updates on product/project activities to key internal/external stakeholders when requested. Role Requirements Qualifications & technical skills • A minimum of a bachelor s degree in pharmacy degree • Years of Experience: 0-1 Years in Pharmaceutical/ Personal Healthcare Regulatory Experience • Language: Arabic/English • Location: Dubai /UAE Soft skills • Experience in Pharma and/or Consumer Healthcare products • Excellent Oral & written communication skills • Team activity, collaborative individual and must have the ability to establish relationships across departments to handle and deliver departmental result Job Qualifications • A minimum of a bachelor s degree in pharmacy degree • Years of Experience: 0-1 Years in Pharmaceutical/ Personal Healthcare Regulatory Experience • Language: Arabic/English • Location: Dubai /UAE Job Schedule Full time Job Number RPHONE_NUMBER Job Segmentation Entry Level • A minimum of a bachelor s degree in pharmacy degree • Years of Experience: 0-1 Years in Pharmaceutical/ Personal Healthcare Regulatory Experience • Language: Arabic/English • Location: Dubai /UAE Soft skills • Experience in Pharma and/or Consumer Healthcare products • Excellent Oral & written communication skills • Team activity, collaborative individual and must have the ability to establish relationships across departments to handle and deliver departmental result