Lead Regulatory Affairs

Would you like to further expand and professionalize the Regulatory Affairs team of QbD? What are your responsibilities? - You are the lead of the internal regulatory professional team and are in the driver’s seat of regulatory policy and strategy for assigned projects - You attract multiple projects with different customers - You keep track of the ever-changing legislation in all the regions - You provide regulatory advice to project teams - The RA lead makes decisions regarding work processes or operational plans, follows budget allocations and keeps stakeholders informed on project resourcing Who are we looking for? - You have at least 10 years of experience in regulatory affairs in the life sciences industry - You have proven 3-5 years in a leadership role with strong management skills. - You have profound knowledge of the relevant national and international legislation, procedural regulations and technical regulations QbD is a healthy company with a strong growth and international ambitions. In addition to a very attractive salary package, we can offer you the following advantages: - Our CEO, Bart Van Acker, became Flemish Young Entrepreneur of 2019, which means that you’ll be part of a vibrant, entrepreneurial organization. - A company with a clear strategy and ambition. - Our HR Business Partners follow you closely, giving you the opportunity to shape your career. - Thanks to our flat organization, we have short communication lines and you can always come to us. - With our extensive training package and our periodic knowledge-sharing moments, we offer you many opportunities to continuously learn, to expand or specialize your knowledge and skills and to gain new expertise. - Get to know your colleagues outside the work environment! Teambuilding and fun activities are planned on a monthly basis. Interested? Send your CV and motivation letter to jobs@qbd.eu. Want some more info? https://jobs.qbd.eu/en/vacancies/vacancy-regulatory-affairs-consultant/