Projects Radioprotection Specialist (f/m/d)
Le seguenti informazioni forniscono una panoramica delle competenze, delle qualità e delle qualifiche necessarie per questo ruolo.
Job ID: 502734
Posted since: 14-Apr-2026
Company: Siemens Healthineers AG
Mid-level Professional
Job type: Full-time
Hybrid (Remote/Office)
Employment type: Permanent
Location(s): Erlangen (Germany), Venafro (Italy), Barcelona (Spain)
Role Overview
Lead radiation protection activities across site design, licensing, shielding, regulatory compliance, and project delivery for new and existing radiopharmaceutical facilities.
Tasks and responsibilities
* Work in cross‐departmental collaboration from site design through start‐up, leading the development of all relevant radiation safety and EHS processes and procedures.
* Generate, submit, and manage radioactive materials licensing documentation, including all required regulatory correspondence.
* Develop shielding designs for new facilities, new applications, and new cyclotron installations.
* Conduct shielding verification and confirmatory surveys.
* Provide onsite support to ensure correct implementation of radiation protection and EHS programs required for successful site operation.
* Review and submit all required decommissioning documentation.
* Provide onsite support as the licensee stakeholder to ensure successful execution of decommissioning activities.
* Manage projects to ensure all required deadlines are met.
* Support sites during regulatory inspections to help secure and maintain regulatory approvals.
Qualifications and experience
* Hold a Masters degree in Medical Physics, Radiological Health, Radiation Protection, Engineering, Chemistry, Pharmacy, or a related scientific field.
* Possess solid familiarity with radioactive materials and EHS regulatory frameworks, ideally gained in regulated industrial or pharmaceutical environments.
* Have several years of experience working in radiochemical or radiopharmaceutical operations, or in applied radiation protection involving unsealed radioactive materials.
* Demonstrate a strong understanding of GMP‐regulated environments and associated regulatory expectations.
* Possess demonstrated project management experience, with the ability to manage timelines, priorities, and cross‐functional deliverables effectively.
* Show a high level of proficiency with Microsoft 365 tools.
* Considered competent if holding a bachelor's degree or a completed vocational education and training combined with additional relevant professional experience in this field.
Attributes and skills
* Excellent written and verbal communication skills, enabling clear translation of technical and regulatory concepts for diverse stakeholders.
* Demonstrate a collaborative and proactive mindset, working effectively in cross‐functional and remote team environments while maintaining high personal accountability.
* Comfortable operating in a hybrid work environment.
* Fluent in English; additional language skills considered a strong asset.
* Flexible and willing to travel up to 30% annually across Europe, the UK, and India.
* Willing to reside in Germany, France, Spain, or Italy, or to relocate if required. xrdztoy
As an equal opportunity employer, we welcome applications from individuals with disabilities.