Manufacturing Technology Transfer Expert M H/F Siemens Healthineers

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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.

Join us as a Technology Transfer Expert and help us shape the future of precision theranostics while advancing patient care.

As part of Global Tech Ops team, you will play a key role in bringing innovative processes, equipment, and methods into our PET manufacturing network. This role offers a unique opportunity to work at the crossroads of Engineering, Quality and MS&T (Manufacturing, Science and Technology), driving impactful improvements to safety, efficiency, and GMP compliance.

This role can be located in France, Spain, or Portugal.

Your role:

- Lead endtoend Technology Transfer projects, managing timelines, deliverables, and crossfunctional 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 closeout.
- Support and contribute to training activities for new equipment, methods, and processes.
- Ensure site readiness posttransfer, 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.

Your expertise:

- 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. Check our Careers Site at

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

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