Do you want to help create the future of healthcare? Our name, Siemens Healthineers, was selected to honor our people who dedicate their energy and passion to this cause. It reflects their pioneering spirit combined with our long history of engineering in the ever-evolving healthcare industry.
We offer you a flexible and dynamic environment with opportunities to go beyond your comfort zone in order to grow personally and professionally. Sounds interesting?
Then come and join our global team as Project Radioprotection Specialist (f/m/d) and help us shape the future of precision theranostics while advancing patient care. This is a role well suited to an ambitious professional, looking for the next step in their career, with the opportunity to lead radiation protection activities across site design, licensing, shielding, regulatory compliance, and project delivery for new and existing radiopharmaceutical facilities.
Choose the best place for your work – Within the scope of this position, it is possible, in consultation with your manager, to work mobile (within Germany) up to an average volume of 60% of the respective working hours.
Even more flexibility? Mobile working from abroad is possible for up to 30 days a year under certain conditions and in selected countries.
This position can be filled in Erlangen (Germany), Venafro (Italy), Barcelona (Spain).
Your tasks and responsibilities:
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You will work in close cross‑departmental collaboration from site design through start‑up, leading the development of all relevant radiation safety and EHS processes and procedures.
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You will be responsible for the generation, submission, and ongoing management of radioactive materials licensing documentation, including all required regulatory correspondence.
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You will develop shielding designs for new facilities, new applications, and new cyclotron installations.
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You will conduct shielding verification and confirmatory surveys.
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You will provide onsite support to ensure the correct implementation of radiation protection and EHS programs required for successful site operation.
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You will review and submit all required decommissioning documentation.
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You will provide onsite support as the licensee stakeholder to ensure successful execution of decommissioning activities.
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You will manage projects to ensure that all required deadlines are met.
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You will support sites during regulatory inspections to help secure and maintain regulatory approvals.
To find out more about the specific business, have a look at Radiopharma
Your qualifications and experience:
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You hold a Masters degree in Medical Physics, Radiological Health, Radiation Protection, Engineering, Chemistry, Pharmacy, or a related scientific field.
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You bring solid familiarity with radioactive materials and EHS regulatory frameworks, ideally gained in regulated industrial or pharmaceutical environments.
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You have several years of experience working in radiochemical or radiopharmaceutical operations, or in applied radiation protection involving unsealed radioactive materials.
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You demonstrate a strong understanding of GMP‑regulated environments and associated regulatory expectations.
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You possess demonstrated project management experience, with the ability to manage timelines, priorities, and cross‑functional deliverables effectively.
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You show a high level of proficiency with Microsoft 365 tools.
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We also welcome candidates with a bachelor’s degree or a completed vocational education and training, combined with additional relevant professional experience in this field.
Your attributes and skills:
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You have excellent written and verbal communication skills, enabling you to clearly translate technical and regulatory concepts for diverse stakeholders.
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You demonstrate a collaborative and proactive mindset and are able to work effectively in cross‑functional and remote team environments while maintaining a high level of personal accountability.
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You are comfortable operating in a hybrid work environment.
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You are fluent in English; additional language skills are considered a strong asset.
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You are flexible and willing to travel up to 30% annually across Europe, the UK, and India.
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You are willing to reside in Germany, France, Spain, or Italy, or to relocate if required.
Our global team:
Siemens Healthineers is a leading global medical technology company. 74,000 dedicated colleagues in over 70 countries are driven to shape the future of healthcare. An estimated 5 million patients across the globe benefit every day from our innovative technologies and services in the areas of diagnostic and therapeutic imaging, laboratory diagnostics and molecular medicine, as well as digital health and enterprise services.
Our culture:
Our culture embraces different perspectives, open debate, and the will to challenge convention. Change is a constant aspect of our work. We aspire to lead the change in our industry rather than just react to it. That’s why we invite you to take on new challenges, test your ideas, and celebrate success. Check our Careers Site at https://www.siemens-healthineers.com/de/careers
As an equal opportunity employer, we welcome applications from individuals with disabilities.#myabilityshs
Wish to find out more before applying? Contact us: [email protected], if you wish to discuss any initial questions with our recruitment team. The contact person handling this job ad is SALIMA BOURHANI.
We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. We ask instead that you create a profile in our talent community where you can upload your CV. Setting up a profile lets us know you are interested in career opportunities with us and makes it easy for us to send you an alert when relevant positions become open. Click here to get started.
To all recruitment agencies:
Siemens Healthineers' recruitment is internally managed, with external support permitted only when a qualified supplier has established a formal contract with us. Unsolicited candidate submissions and referrals, absent a current supplier contract, do not establish consent and are ineligible for fees. We delete and destroy unsolicited information, thus, would recommend you refrain from any such practices. Your adherence to our policies is appreciated.
