Technology Transfer Specialist – Biotech Manufacturing (m/w/d) About Our Client For our client, a leading biopharmaceutical company specializing in cutting‑edge biologics drug substance manufacturing for early‑phase clinical supply, we are seeking a Technology Transfer Specialist (m/w/d). This state‑of‑the‑art biotech facility operates with a flexible, multi‑product strategy integrating the latest technologies into the clinical pipeline to enable rapid, agile product launches and drive innovation in biologics‑based medicine development.
Your Responsibilities
Drive the
introduction of new biological products
into manufacturing by coordinating schedules and ensuring tasks are completed on time and right‑first‑time
Prepare and manage
GMP‑compliant documentation
such as risk assessments, change controls, batch records, sampling plans, and Bills of Material (BOMs)
Maintain and update data across
digital manufacturing systems
including SAP COMET, MES, and DeltaV
Develop and support
process descriptions, facility fit analyses, and process models
for continuous and fed‑batch manufacturing processes
Contribute to the design and rollout of
best practices in tech transfer , with a focus on streamlining and reducing risk towards fully digitized workflows
Author, review, and maintain
SOPs, Work Instructions, Electronic Batch Records (EBRs/gBMRs)
and related manufacturing documents
Apply strong
analytical and problem‑solving skills
to support cross‑functional and global teams in resolving technical challenges
Your Profile
Degree in a scientific or technical discipline
(e.g. Biology, Chemistry, Biotechnology, Engineering, or related field)
Minimum 5 years of professional experience
in the pharmaceutical or biotech industry, ideally in a GMP‑regulated biologics drug substance manufacturing environment
Hands‑on experience with
digital and automation systems
such as DeltaV, MES, eVal, and SAP COMET
Solid understanding of
cGMP regulations
and the principles of New Product Introduction / Technology Transfer
Familiarity with
mAb unit operations
and experience with single‑use manufacturing systems is a plus
Proven ability to
manage small projects
within cross‑functional teams, including basic project management skills
Fluent in English
(written and spoken, minimum B1); German language skills are an advantage
Collaborative team player with a proactive mindset and a genuine drive for
continuous improvement and learning
#J-18808-Ljbffr
Your Responsibilities
Drive the
introduction of new biological products
into manufacturing by coordinating schedules and ensuring tasks are completed on time and right‑first‑time
Prepare and manage
GMP‑compliant documentation
such as risk assessments, change controls, batch records, sampling plans, and Bills of Material (BOMs)
Maintain and update data across
digital manufacturing systems
including SAP COMET, MES, and DeltaV
Develop and support
process descriptions, facility fit analyses, and process models
for continuous and fed‑batch manufacturing processes
Contribute to the design and rollout of
best practices in tech transfer , with a focus on streamlining and reducing risk towards fully digitized workflows
Author, review, and maintain
SOPs, Work Instructions, Electronic Batch Records (EBRs/gBMRs)
and related manufacturing documents
Apply strong
analytical and problem‑solving skills
to support cross‑functional and global teams in resolving technical challenges
Your Profile
Degree in a scientific or technical discipline
(e.g. Biology, Chemistry, Biotechnology, Engineering, or related field)
Minimum 5 years of professional experience
in the pharmaceutical or biotech industry, ideally in a GMP‑regulated biologics drug substance manufacturing environment
Hands‑on experience with
digital and automation systems
such as DeltaV, MES, eVal, and SAP COMET
Solid understanding of
cGMP regulations
and the principles of New Product Introduction / Technology Transfer
Familiarity with
mAb unit operations
and experience with single‑use manufacturing systems is a plus
Proven ability to
manage small projects
within cross‑functional teams, including basic project management skills
Fluent in English
(written and spoken, minimum B1); German language skills are an advantage
Collaborative team player with a proactive mindset and a genuine drive for
continuous improvement and learning
#J-18808-Ljbffr
Technology Transfer Specialist Arbeitgeber: nemensis ag Schweiz
Unser Kunde ist ein innovatives und international ausgerichtetes Biotech-Unternehmen in der Region Luzern, das sich durch eine dynamische Arbeitsumgebung und ein starkes Engagement für kontinuierliche Innovation auszeichnet. Die Mitarbeiter profitieren von einer offenen Unternehmenskultur, die Teamarbeit und persönliche Entwicklung fördert, sowie von attraktiven Weiterbildungsmöglichkeiten und einem flexiblen Arbeitszeitmodell. Hier haben Sie die Chance, Ihre GMP-Expertise in einem zukunftsorientierten Umfeld einzubringen und aktiv an der Gestaltung der biologischen Arzneimittelproduktion mitzuwirken.
