Senior Global Technology Transfer Lead

Senior Global Technology Transfer Lead 80-100%

The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

Step into the role of Senior Technology Transfer Lead in Global MSAT Drug Product, driving complex end‑to‑end drug product transfers from development through PPQ, regulatory filing, inspection readiness, and commercial launch. As the process owner, you’ll lead harmonization and standardization across sites while overseeing process setup, scale‑up, GMP change management, and on‑site technical support during execution. Serving as the primary technical contact, you’ll guide manufacturing strategy, ensure compliance with global standards, and enable the seamless transfer and implementation of high‑impact projects.

• Drive high‑complexity drug product commercial transfers for assigned projects, leading activities from New Product Introduction through PPQ, regulatory filing, pre‑approval health authority inspections, and first commercial launch.
• Serve as the primary technical point of contact for all technology‑transfer‑related manufacturing topics within internal and customer project teams.
• Define and monitor project scope, timing and progress of assigned stages.
• Lead process setup, scale‑up, and implementation activities at GMP drug product manufacturing sites, including on‑site technical support during batch execution.
• Responsible for new product introduction, process implementation, process control strategy and technical transfer and process validation documentation, including review of dossier modules for regulatory filing.
• Drive GMP change management strategy of assigned projects and initiate and manage GMP change control in system.
• Lead and support critical GMP product/process deviations and corresponding implementation of corrective/preventive actions (CAPAs).
• Ensure all activities are performed according to current standards (Good Manufacturing Practice, Health Safety Environment, Regulatory etc.).

• MSc, PhD or equivalent in a relevant scientific or engineering field (e.g., Pharmaceutical Sciences, Biochemistry, Bioengineering, Pharmaceutical Engineering).
• Extensive experience in biotech / pharma / CDMO industry; specifically with technology transfer of aseptic product manufacture of protein drug products filled into vials or syringes.
• Experience with drug product development.
• Experience with lyophilization process is highly desirable. Experience with highly‑potent drug products is desirable.
• Proven ability to lead cross‑functional teams and maintain a team mentality.
• Exemplary planning and organizing skills, including project management, risk management, interpretation and communication of complex scientific data, technical writing skills.
• Excellent communication skills and command of English both written and oral. German is an advantage.
• Ability to navigate technical challenges, support investigations, and drive effective execution in a fast‑paced setting.

• Competitive salary and compensation programs that recognize high performance.
• Lifestyle, family, and leisure benefits tailored to local needs.
• Agile career and dynamic work culture.
• Highly collaborative environment that fosters teamwork and inclusion.
• Inclusive and ethical workplace.

With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together.