Regulatory Affairs Lead owning regulatory strategy and safety oversight for assigned products in the Levant. Collaborating with cross-functional teams and ensuring compliance with local and global regulations.
Responsibilities
own regulatory strategy and safety oversight for assigned products and projects
lead regulatory submissions and approvals- prepare, product registrations and amendments, and respond to health authority queries
ensure compliance and governance- maintain adherence to global and local regulatory standards, conduct reviews and audits, and manage compliance risks
oversee pharmacovigilance activities: supervise collection, analysis and reporting of safety data, identify new safety signals and ensure timely regulatory reporting
collaborate with stakeholders, partner with clinical, safety, commercial and external partners, and act as the company’s regulatory and safety contact for health authorities and policymakers
monitor regulatory trends and adapt strategy, track regulatory changes, assess impact, and develop approaches to maintain compliance and accelerate approvals
Requirements
Bachelor degree as a minimum in a life science or medical discipline (e.g., MD, PharmD. Pharmacy)
5–7+ years’ experience in regulatory affairs within the multinational pharmaceutical industry
Proven track record managing regulatory submissions, compliance activities and safety data analysis
Experience engaging with health authorities and leading cross‑functional regulatory or safety initiatives
Strong knowledge of global and local regulatory frameworks
Excellent attention to detail, problem‑solving skills, and the ability to communicate complex regulatory and safety information clearly
Proficiency in English (written and spoken)
Benefits
opportunities to learn and develop are all around us
benefits are designed with your career and life stage in mind
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