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We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Ramboll Group A/S. As a key member of our Health Sciences service line, you will play a crucial role in supporting our clients in the chemicals industry with their product regulatory compliance and stewardship needs.
Key Responsibilities- Provide technical support to clients and colleagues on issues relating to product regulatory compliance and stewardship in Spain
- Participate in projects relating to REACH, BPR, and other EU regulations
- Collaborate with colleagues to advance product authorization and active substance approval files in a timely and effective manner
- Work with the team to carry out dossiers according to ECHA standards
- Collaborate with Senior Consultants in Health Sciences
- Participate in activities prior to projects, such as developing authorisation strategies and regulatory advice for clients
- Strong academic background with a relevant science-based degree (e.g. biology, chemistry, biochemistry, pharmacology)
- Minimum of 2 years' experience working in regulatory affairs or product safety, ideally in the chemicals industry
- Knowledge of European regulations (REACH, BPR, and other RoHS directives)
- Experience of carrying out Risk Assessments (Environmental, biological, human)
- Experience of using ECHA IT tools and portals: REACH IT, IUCLID, SPS Editor, SCIP
- Fluency in written and verbal English is essential; knowledge of French, Portuguese, or other languages highly desirable
As a Regulatory Affairs Specialist at Ramboll Group A/S, you will have the opportunity to work on challenging and inspiring projects within an environment that is friendly, flexible, open, and supportive. You will be part of a global company that has been growing successfully since its founding in 1945, and you will have the chance to develop your skills and expertise in a dynamic and collaborative team.