Manufacturing Technology Transfer Expert (m/f/d)

Manufacturing Technology Transfer Expert (m/f/d)

Any Siemens Healthineers location in

• France
• Italy
• Portugal
• Spain

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, Italy, Spain, or Portugal.

Your role:

• 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.

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.

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