Specialist Tech Transfer

Headhunter: LHH

Biotechnology

Luzern - Schweiz

Senior Specialist / Project Manager

Hybrid

Experteer Overview

In this role you will support Tech Transfer activities for New Product Introduction within the Manufacturing Operations team in Luzern. You will help shape the site tech transfer strategy and ensure on-time, right-first-time delivery across cross-functional teams. You will work with GMP documentation and digital manufacturing systems to drive process improvements and knowledge sharing. The position emphasizes quality, compliance, and safety as you enable scalable tech transfer in a biotech/pharma environment.

Responsibilites

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

Key requirements

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