StrongCompany Descriptionbr/strongFor over 30 years, Lesaffre has been involved in Human Health Nutrition as part of its ambition to Better Nourish and Protect the Planet. In November 2018, Lesaffre acquired Gnosis Advanced Biotech and officially combined it with Lesaffre Human Care to form a new Business Unit named strongGnosis by Lesaffre /strong.brAt strongGnosis by Lesaffre /strong, we are committed to cultivating and to delivering nutritional actives, probiotics, and nutritional and functional yeasts that benefit human health and wellbeing, thanks to the power of microorganisms and biotransformation processes like fermentation. Put differently, we explore life to improve living.brOur vision: At strongGnosis by Lesaffre /strong, we strive for a world that moves better, digests better, ages better, feels better, and, ultimately, lives better thanks to microorganisms and biotransformation.brstrongJob Descriptionbr/strongAt Gnosis by Lesaffre, we are looking for a talented, dynamic, and motivated Regulatory Affairs Specialist to support the expansion of our business. You will be responsible for the regulatory compliance of our product portfolio and play a critical role providing strategic advice on regulatory risks and opportunities to support market growth and innovation.brstrongResponsibilitiesbr/strongulliEnsure compliance of assigned Gnosis’ product portfolio with local regulations, /liliManage timely regional registration activities, including registration dossier preparation and proper documentation of submitted documents, /liliExecute regional regulatory strategies in line with the global strategic plan, /liliProvide regulatory guidance and advice to internal stakeholders (e.g. marketing, RD), /liliConduct regulatory watch and monitor changes in local legislation landscape, assess the impact towards Gnosis’s product portfolio and communicate accordingly to internal stakeholders, /liliBuild effective working relationships with internal stakeholders, /liliWork closely with regulatory colleagues to maintain knowledge in local regulations and product-specific regulatory requirements, /liliMaintain full awareness of regulatory activities of assigned portfolio and provide regular reports.br/li /ulQualificationsbrulliBachelor’s degree or equivalent in Science, Pharmacy or related scientific discipline /liliMinimum of 2 years of regulatory experience in healthcare or food industry. /liliKnowledge in food/food supplements in EU/US, experience with EFSA regulations is a plus, /liliGood organizational skills, possess structured approach to working tasks, /liliCollaborative team player with the ability to work independently, /liliExperience in project management appreciated, however project management course will be offered, /liliComfortable working in an international fast paced environment, /liliGood written and verbal communication skills, /liliFluent in English is a must.br/li /ulAdditional InformationbrulliThe job is based in Desio (MB) - Italy /liliFull-time contract /liliPossible Smart-Working after trial period /liliBe part of a growing company /liliWork in a dynamic international environment /liliWe are a successful family-owned company with long-standing history where people truly matter. /liliWe promote a sense of fulfilment with a genuine mission: nourish and protect the planet. /liliAn opportunity to work in a real international environment.br/li /ulemAt Lesaffre, diversity is a strength that enriches our culture and our teams. We are committed to offering you a work environment where you can thrive, regardless of your background, gender, age or abilities. We encourage all applications, as we believe that diverse perspectives strengthen our ability to innovate and meet the challenges of tomorrow. /em #J-18808-Ljbffr