Ph3Projects Radioprotection Specialist (f/m/d) /h3 pJob ID: /p pPosted since: 14-Apr-2026 /p pCompany: Siemens Healthineers AG /p pMid-level Professional /p pJob type: Full-time /p pHybrid (Remote/Office) /p pEmployment type: Permanent /p pLocation(s): Erlangen (Germany), Venafro (Italy), Barcelona (Spain) /p h3Role Overview /h3 pLead radiation protection activities across site design, licensing, shielding, regulatory compliance, and project delivery for new and existing radiopharmaceutical facilities. /p h3Tasks and responsibilities /h3 ul liWork in cross‑departmental collaboration from site design through start‑up, leading the development of all relevant radiation safety and EHS processes and procedures. /li liGenerate, submit, and manage radioactive materials licensing documentation, including all required regulatory correspondence. /li liDevelop shielding designs for new facilities, new applications, and new cyclotron installations. /li liConduct shielding verification and confirmatory surveys. /li liProvide onsite support to ensure correct implementation of radiation protection and EHS programs required for successful site operation. /li liReview and submit all required decommissioning documentation. /li liProvide onsite support as the licensee stakeholder to ensure successful execution of decommissioning activities. /li liManage projects to ensure all required deadlines are met. /li liSupport sites during regulatory inspections to help secure and maintain regulatory approvals. /li /ul h3Qualifications and experience /h3 ul liHold a Masters degree in Medical Physics, Radiological Health, Radiation Protection, Engineering, Chemistry, Pharmacy, or a related scientific field. /li liPossess solid familiarity with radioactive materials and EHS regulatory frameworks, ideally gained in regulated industrial or pharmaceutical environments. /li liHave several years of experience working in radiochemical or radiopharmaceutical operations, or in applied radiation protection involving unsealed radioactive materials. /li liDemonstrate a strong understanding of GMP‑regulated environments and associated regulatory expectations. /li liPossess demonstrated project management experience, with the ability to manage timelines, priorities, and cross‑functional deliverables effectively. /li liShow a high level of proficiency with Microsoft 365 tools. /li liConsidered competent if holding a bachelor’s degree or a completed vocational education and training combined with additional relevant professional experience in this field. /li /ul h3Attributes and skills /h3 ul liExcellent written and verbal communication skills, enabling clear translation of technical and regulatory concepts for diverse stakeholders. /li liDemonstrate a collaborative and proactive mindset, working effectively in cross‑functional and remote team environments while maintaining high personal accountability. /li liComfortable operating in a hybrid work environment. /li liFluent in English; additional language skills considered a strong asset. /li liFlexible and willing to travel up to 30% annually across Europe, the UK, and India. /li liWilling to reside in Germany, France, Spain, or Italy, or to relocate if required. /li /ul pAs an equal opportunity employer, we welcome applications from individuals with disabilities. /p /p #J-18808-Ljbffr