Qualified Person
Pubblicato il 27-09-2026 - Ith Icoserve in Colleretto Giacosa
Job ID
515837
Posted since
31-Jul-2026
Field of work
Quality Management
Company
Mid-level Professional
Job type
Full-time
Office/Site only
Employment type
Permanent
Location(s)
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.
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.
Compensation: €39,000 - €52,000 base salary + benefits
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 d