Regulatory Affairs Specialist

Regulatory Affairs Specialist (Hybrid/Remote – Egypt, 12-Month FTC)Contract: 12-Month Fixed-Term Contract, EgyptStart: To be Confirmed (Pipeline Opportunity)Organisation: Leading global life sciences company (via Kelly FSP)About the RoleKelly is pipelining talent for an evergreen Regulatory Affairs role in pharma. If you’re looking for a project-based career in Regulatory Affairs, we’d love to have a preliminary conversation, connect with us to explore future opportunities!This is a pipeline opportunity for proactive candidates interested in joining a global leader in the life sciences industry. The Regulatory Affairs Specialist will provide critical support for regulatory operations, data management, and compliance activities within a collaborative, international environment. You will work closely with cross-functional teams and maintain regulatory data and documentation across multiple global markets.Key ResponsibilitiesMaintain, validate, and report regulatory information in RIM systems and related databases.Coordinate and monitor regulatory activities and submissions in international markets.Support reporting and analysis for business decision-making.Review, process, and ensure accuracy of regulatory data and systems.Execute procedures according to SOPs and support audit readiness.Drive improvements in data quality, reporting, and operational efficiency.Required Experience & SkillsBackground in Regulatory Affairs, Operations, or Administration within life sciences.Industry experience in pharmaceuticals, biotechnology, medtech, or regulated environments.Strong recordkeeping, attention to detail, and organisational skills.Advanced Microsoft Excel abilities (Pivot Tables, lookups, data analysis).Professional English and the ability to coordinate multiple tasks in a regulated, fast-paced setting.Experience supporting operational or compliance-driven environments.Technical SkillsMicrosoft Excel (advanced), Word, Outlook, PowerPoint.Familiarity with regulatory/business systems and reporting tools (experience with Power BI is a bonus).Must-HavesBachelor’s degree in Life Sciences, Pharmacy, Chemistry, Biotechnology, Biomedical Sciences, or related.Experience with regulatory/business data in structured systems.Excellent detail orientation, organisational, and communication skills.Comfortable with process-driven work and international collaboration.Nice-to-HavesExperience with Regulatory Information Management (RIM) systems.Global or regional regulatory operations experience.Exposure to product lifecycle management or regulatory change.Experience producing dashboards/reports (Excel or Power BI).Project or regulatory tracking experience.Working ArrangementHybrid work model (Egypt).Full-time, 12-month Fixed-Term Contract.Collaboration with global regulatory teams.Why Join?Opportunity to join a globally recognised life sciences company through Kelly’s FSP model.Work with international experts on high-impact projects.Gain global exposure and expand your regulatory knowledge.Be part of a collaborative, growth-focused work culture.Pipeline opportunity with anticipated hiring in the near future, apply early to be considered once the position is formally approved and released.