At Siemens Healthineers (SHS) Radiopharma, we are committed to driving sustainable progress through cutting-edge technology. We empower our customers by bridging the physical and digital worlds—enhancing the way we live, work, and move, today and for future generations. 

We believe that business success begins with our people. That’s why we prioritize a culture where individuals thrive. Our diverse team is ready to support, inspire, and challenge you to grow in new and meaningful ways. Together, there are limitless possibilities of where our shared journey may lead.

As the global leader in the supply of positron emission tomography (PET) radiopharmaceuticals, SHS Radiopharma pioneered the commercial PET radiopharmacy model over 30 years ago—and continues to shape the future of molecular imaging.

We are seeking an experienced and driven professional to join our Radiopharma business as a Qualified Person (QP), and take legal responsibility for ensuring that radiopharmaceutical products are manufactured, tested, and released in full compliance with EU GMP requirements, radiation safety regulations, and Marketing Authorization requirements before being supplied for clinical or commercial use.

Location: Colleretto Giacosa (TO), Italy

Your role: 

• Certify and release radiopharmaceutical batches in accordance with EU Directive 2001/83/EC and applicable national legislation. 
• Ensure manufacturing and quality control activities comply with GMP requirements and radiation safety regulations. 
• Review and approve batch documentation, deviations, CAPAs, change controls, and quality investigations. 
• Collaborate closely with Production, Quality Control, Quality Assurance, and Radiation Safety teams to ensure product quality, integrity, and compliance. 
• Act as the primary contact for product release activities during regulatory inspections and customer audits. 
• Monitor regulatory developments and ensure continued site compliance with applicable requirements. 
• Participate in risk assessments and investigations involving radioactive materials. 
• Provide expert advice on GMP, quality, and regulatory topics to internal stakeholders. 
• Ensure personnel involved in manufacturing and quality control activities receive appropriate GMP and radiation safety training.

Your profile:

• Degree in Pharmacy or CTF (Chemistry and Pharmaceutical Technology). 
• State Pharmacy Qualification required in Italy. 
• Fluent Italian and English, both written and spoken. 
• 3 to 5 years of experience in Quality Control and/or Quality Assurance within a GMP-regulated pharmaceutical environment. 
• Experience in radiopharmaceuticals, sterile manufacturing, or aseptic processing is highly desirable. 
• Strong knowledge of EU GMP regulations and pharmaceutical quality systems. 
• Excellent analytical skills, attention to detail, and ability to make quality-critical decisions. 
• Strong communication and stakeholder management skills within a cross-functional environment.

Who we are:  
 We are a team of more than 74,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways. 

How we work: 
 When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Check our Careers Site at Jobs at Siemens Healthineers AG

As an equal opportunity employer, we welcome applications from individuals with disabilities. 

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. Please create a profile within our talent community and subscribe to personalized job alert that will keep you posted about new opportunities. 

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.