Technology Transfer Specialist – Biotech Manufacturing (m/w/d) 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). The state‑of‑the‑art biotech facility operates with a flexible, multi‑product strategy that integrates the latest technologies into the clinical pipeline to enable rapid, agile product launches and drive innovation in biologics‑based medicine development.
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, focusing on streamlining and reducing risk toward 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.
Qualifications
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.
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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, focusing on streamlining and reducing risk toward 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.
Qualifications
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 – Biotech Manufacturing Arbeitgeber: nemensis ag
Als Leiter RX-Aussendienst in einem etablierten Schweizer Pharmaunternehmen profitieren Sie von einer flexiblen Home-Office-Regelung und einem unterstützenden Arbeitsumfeld, das auf kontinuierliche Weiterbildung und persönliche Entwicklung setzt. Das Unternehmen bietet Ihnen die Möglichkeit, ein engagiertes Team zu führen und aktiv zur Verbesserung des Schweizer Gesundheitsmarktes beizutragen, während Sie von einem breiten Produktportfolio und einem starken Netzwerk innerhalb der Branche profitieren.
