Manufacturing Technology Transfer Expert (m/f/d)

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.

Technology Transfer Expert

Role can be located in France, Italy, Spain, or Portugal.

Responsibilities

• Lead end‑to‑end Technology Transfer projects, managing timelines, deliverables, and cross‑functional coordination: MS&T, Quality, TRD (Research & Development), Engineering, IT, suppliers, and external partners.
• Define qualification and validation strategies for new QC/production processes and equipment across Radiopharma network, in alignment with MS&T, Global Tech Ops, and Quality.
• Oversee the preparation and execution of qualification documentation (IQ/OQ/PQ) and ensure proper installation and validation activities.
• Drive technology scouting with Engineering to identify, source, and test new solutions that enhance process efficiency while meeting Safety, GMP, and Annex 1 requirements.
• Ensure strong collaboration and stakeholder alignment throughout the project lifecycle — from initiation and planning to execution and close‑out.
• Support and contribute to training activities for new equipment, methods, and processes.
• Ensure site readiness post‑transfer, covering equipment, methods, and processes.
• Participate in local/global change control and implementation of action plans.
• Contribute to SOP development for manufacturing and QC operations.
• Harmonize and distribute qualification documentation across PET manufacturing sites.
• Act as a Subject Matter Expert (SME) during GMP inspections and serve as a key point of contact for your scope.

This role requires occasional travel across Europe, approximately one week per month.

Qualifications

• Bachelor’s or Master’s degree in Chemistry, Pharmacy, or any related field.
• Minimum 3 years experience in pharmaceutical production or quality control within highly regulated environments.
• Solid understanding of sterile process design and strong familiarity with EU GMP requirements—particularly Annex 1.
• Ability to understand and navigate complex technical activities, processes, and equipment.
• Excellent written and spoken English, with strong interpersonal skills that enable effective collaboration across diverse teams and stakeholders.

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.

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