Regulatory Affairs Officer - Life Sciences (Flanders)

ALTEN Belgium is a leading consultancy company in the fields of Life Sciences, Engineering and IT in which our people and clients are central.In our open and adaptable organization, we get the best out of our ambitious employees enabling them to perform optimally. We do this by offering them the most challenging projects, but also to continuously acquire new expertise to boost their careers. This can be done with the help of our ALTEN Academy, but also through our knowledge sharing events.All employees together form a large network of expertise, even at an international level. In this way we offer optimal growth to our consultants and the best solutions for our customers.We are currently looking for a Regulatory Affairs Officer to join our Life Sciences team in Belgium. The Regulatory Affairs Officer will manage the preparation, submission, and maintenance of local registrations for various products including biocides, cleaners, veterinary drugs, complementary feed products, and cosmetics. In addition, the Regulatory Affairs Officer ensures compliance with relevant requirements in different countries.Main responsibilitiesRegulatory Compliance: Regulatory watch on the latest developments in regulations for different products and countries. Ensure all products meet applicable safety, efficacy, and labeling local standards;Registration & Dossier Management: Prepare registration dossiers and declarations/notifications, ensuring timely submissions to official bodies for new registrations, renewals, and updates;Maintenance of records of all regulatory submissions, approvals, and renewals.Liaison & Communication: Act as the primary contact with local regulatory authorities.Collaborate with the sales team, various functions including Marketing & RD&E, … and distributors to facilitate effective communication and alignment on regulatory activities. Provide concise and informative activity reports to management;Training & Advisory: Provide regulatory guidance to internal teams.Your profileBachelor’s or master’s degree in disciplines such as chemistry, biochemistry, pharma, quality, or project management, with at least 3 years of proven experience in regulatory affairs or project management and problem-solving;Familiarity with national regulatory frameworks for biocides, veterinary medicines, and complementary feed;Excellent organizational skills with the ability to manage and prioritize multiple tasks concurrently, project management and problem-solving skills;Flexibility, adaptability, and stress resistant, with a readiness to handle challenges, especially in urgent situations;Good collaboration skills to work effectively within an international and multidisciplinary team;High attention to detail and analytical thinking with a strong sense of synthesis;Proficiency in regulatory software and Microsoft Office Suite, particularly Excel;Fluency in English; knowledge of Dutch and other languages considered a strong advantage.What ALTEN has to offerA permanent contract;A salary package in line with your experience and extra benefits (company car, meal vouchers, recovery days, insurances);The possibility to join a great team and be part of the success story of an international group.We are also open to work with freelancers! Apply now and be a part of our amazing journey. We believe in growing together! We are looking forward to getting to know you and your ambitions!