.We invite you to bring your knowledge of European regulations governing product safety and stewardship into play as you support organisations around the world bring to the market products in a range of uses that meet relevant requirements and are safe for human health and the environment.The ideal candidate will be willing to travel to Barcelona twice a month to meet with colleagues and the client.Are you our new Regulatory Affairs Consultant? Click the I'm Interested-button to send your application.Inviting bright mindsDo you want to push the boundaries of your profession and develop your excellence in an open, collaborative and empowering culture? We work to create a sustainable future and our inspiring projects and innovative solutions aim to set the standard among our peers. You will join a global company that has been growing successfully since its founding in 1945. Together, we lead and leave a positive impact on societies, companies and people around the world.You will join our international Health Sciences service line:As our new expert in biocides, you will be part of an established international team of Product Safety and Stewardship specialists, delivering key knowledge to a range of Ramboll projects. Our regulatory scientists characterise and effectively communicate the potential risks from chemicals and product uses and identify options for safe, state-of-the-science stewardship.Our successful global track record includes evaluations and stewardship for chemical producers, biocides, food and food packaging, building materials, toys, cosmetics, aerospace manufacturing, medical device and electronic device manufacturing, and pesticides.Your key tasks and responsibilities will be:Providing technical support to clients and colleagues on issues relating to product regulatory compliance and stewardship in SpainParticipating on projects relating to REACH, BPR etcCollaborating with colleagues so that the product authorization and active substance approval files advance in a timely and effective mannerWorking with the team to carry out the dossiers according to ECHA standards.Collaborating with the Senior Consultants in Health SciencesParticipating in activities prior to projects (such as offers etc)
