Specialist Tech Transfer

For one of our clients, we are currently seeking an Specialist Tech Transfer (m/w/d) to join their team onsite in Luzern.

The Technology Transfer specialist will be a member of the Manufacturing Operations team, reporting to the Technology Transfer Lead. The successful candidate would be a responsible for supporting New Product Introduction, while also acting as a key contributor to the evolving site tech transfer strategy.

Responsibilities would primarily entail, but are not limited to, the following:

• Support Tech Transfer program development and execution.
• Prepare and manage GMP documentation (risk assessments, change controls, batch records, sampling plans, BOMs).
• Maintain and update data in digital systems (COMET SAP, MES, DeltaV).
• Coordinate new program introductions to ensure on-time, right-first-time delivery.
• Represent Tech Transfer in cross-functional teams and manage small to medium-complexity projects.
• Develop and support Tech Transfer documentation, process models, and best practices.
• Drive continuous improvement, process optimization, and knowledge management initiatives.
• Author and maintain BOMs, EBRs, gBMRs, SOPs, and WIs.
• Apply strong problem-solving skills and collaborate effectively within global, multidisciplinary teams.
• Foster innovation, continuous learning, and the development of future Tech Transfer solutions.
• Follow Safety, Health & Environment standards and promote a strong safety culture.
• Ensure the highest standards of quality, compliance, and safety.

To be successful in this role, you will have the following:

• Degree in a relevant scientific or technical field.
• Minimum 5 years’ experience in the pharmaceutical or biotechnology industry.
• Strong understanding of mAb manufacturing unit operations and Tech Transfer/New Product Introduction principles.
• Basic project management knowledge with experience coordinating cross-functional projects.
• Proficiency in GMP documentation, including BOMs, batch records/sheets, change controls, and risk assessments.
• Experience with digital manufacturing and automation systems such as DeltaV, MES, SAP COMET, and eVal.
• Good knowledge of cGMP requirements and biologics manufacturing environments, ideally involving single-use technologies.
• Strong analytical, troubleshooting, problem-solving, and risk assessment skills.
• Ability to work effectively both independently and within multidisciplinary teams.
• Professional English communication skills (minimum B1); German is an advantage.

Additional Information:

• Site-based role: 5 days per week, 40 hours weekly
•  Long-term temporary contract: From 01/08/2026 to 31/07/2027
• Onsite presence required to fully support the team and operational activities in the greater Lucerne area

 

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