Associate Director, Regulatory Affairs in Genève

pThe Associate Director, Regulatory Affairs leads IFPMA's policy and regulatory strategies on manufacturing innovation, quality systems, good manufacturing practices and reliance while ensuring cross-team integration. In addition, provides technical and functional leadership for strategically relevant regulatory policy areas. In partnership with member companies and industry experts, the role shapes industry positions, advances strategic regulatory policy priorities, and drives initiatives that support a science-based, globally harmonized regulatory environment. /p pReporting to the Director, Scientific Regulatory Affairs, the Associate Director is responsible for leading the Quality Manufacturing and Reliance work programs under the Regulatory Science Committee, building alignment across members and stakeholders, and overseeing the development of policy, advocacy, and technical deliverables. The role represents IFPMA in key external forums and engages senior stakeholders across the regulatory ecosystem to advance industry priorities and strengthen the organization's influence on global regulatory policy. /p h3Key responsibilities /h3 ul liLead the development and implementation of the Quality Manufacturing and Reliance strategies and work program under the IFPMA Regulatory Science Committee. /li liRepresent IFPMA in external regulatory and policy forums, coordinating member briefings, positions, and presentations. /li liShapes industry advocacy and regulatory policy recommendations by synthesizing scientific, technical, and stakeholder input. /li liSupport engagement with multilateral organizations and ensure alignment across IFPMA member associations and industry stakeholders. /li liProvide strategic updates to senior management and contribute actively to cross-functional Regulatory Team initiatives. /li /ul h3Qualifications Requirements /h3 ul liStrong subject matter expertise and strategic thinking skills, with the ability to identify opportunities, align stakeholders, and drive results. /li liExcellent advocacy, communication, presentation, and stakeholder engagement skills. /li liSolid understanding of the pharmaceutical industry and broader public policy environment. /li liProven ability to build and maintain effective relationships with internal and external stakeholders. /li liStrong analytical, project management, and organizational capabilities. /li liExperience working across cross-functional teams and coordinating committees, working groups, and external partners. /li li8-10 years of relevant experience in healthcare policy, public affairs, government affairs, or a related pharmaceutical-sector role. /li liMaster's degree in regulatory science, pharmacy, biochemistry, health policy, public health, or a related field; additional qualifications are an asset. /li liFluent in English (oral and written); other languages (e.g. French) are an asset. /li liCandidate must hold an EU passport or otherwise demonstrate the legal right to work in Switzerland. /li /ul pAs an organization driven by our values of Integrity, Respect and Excellence, IFPMA welcomes diversity and fosters an inclusive workplace where individuals are valued and empowered to thrive. We encourage applications from all qualified candidates regardless of race, gender, ethnicity, sexual orientation, religion, or disability. /p #J-18808-Ljbffr