Job-Support.dk - din genvej til et nyt job!
p, pre, code, blockquote, ul, ol, dl, address Do you want to ensure that the development & marketing of probiotic bacteria is compliant? If you have some years? experience as Regulatory Affairs Specialist in EU food legislation, and you are looking for a job where you can get a broad regulatory responsibility for a highly prioritized business area - this is your opportunity. In Chr. Hansen Human Health you will be part of a very successful international market leader that builds on 140 years? expertise within microbial solutions and food bacteria, and is the leading global supplier of scientifically documented probiotic strains for infant formula, food supplement and health-care companies around the world. We are looking for an engaged and dedicated Regulatory Affairs Specialist to provide regulatory guidance and support to our Human Health Business, mainly focusing on probiotics in food supplements and infant formula. You will be based at our HQ in Hørsholm, Denmark. Main task EU Regulatory Clearance of substances used in production of food supplements / infant formula Regulatory input and review to Product Documentation Regulatory advice & service to EU customers Support to QA regulatory inquiries e.g. hygiene parameters Regulatory lead in New Product Development cross-functional projects teams Regulatory lead in EU focused cross-functional Customer Development Project teams Perform Internal Regulatory trainings to QA, R&D, Marketing and Sales. Excellent communication & collaboration with numerous stakeholders internal and external of the organization Overall responsibility Drive Human health regulatory support to development of new products and maintain existing products and their documentation against EU legislation. To do this you will have a broad range of internal contacts from Commercial Development, Business Support, QA, Innovation and many more. Your personal profile In depth knowledge of EU food legislation Minimum 2-5 years regulatory experience in multinational food/ consumer healthcare company Have a MSc in Life Sciences or similar Pharmaceutical experience desirable but not essential Global regulatory experience is an advantage Good organizational skills, methodical, systematic approach with ability to handle multiple projects simultaneously Strategic thinking and sense for practical solutions Able to work on own initiative, and within a team Ability to travel, although a limited number of trips are to be expected You have multicultural understanding You love to ?deep-dive? into projects and you keep your head above water Great communication and collaboration skills Fluent in English, oral and written ? Danish is a plus What we offer You will be part of a highly motivated, result-driven and solution-oriented Global Regulatory Affairs team. Team work is at the core of our success. You will work for an innovative business with high ambitions and a commitment to continue their sustainable growth journey. For more information If you have any enquiries please contact Global Regulatory Affairs Director Hafiz Choudhury at Tel: +45 60433509; firstname.lastname@example.org Please apply online, click here. Deadline for applications is 21st January 2018. Interviews will be held throughout the application period and we, therefore, urge you to apply as soon as possible. Read more about working for Chr. Hansen at: www.chr-hansen.com/career