Specialist Tech Transfer

LHH Lucerne, Switzerland

Posted 1 day ago Hybrid Job Permanent Competitive

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

Job ID 142CD8CB-08AD-4279-9FA7-658AD2D79AE5

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ABOUT COMPANY

LHH

Lausanne, Switzerland

72 Employees HR & Recruitment

At LHH, we exist to help people, teams, and organizations find and prepare for what’s next. Our end-to-end HR solutions future-proof organizations and...

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