Technology Transfer Engineer - Biopharma & GMP (m/f/d) 100%

• Type of Employment: temporary through nemensis ag, 100%
• ID: 22647
• Duration: 03.03.2025 - 31.07.2026
• Salary: CHF 7300 monthly - CHF 8900 monthly

Responsibilities

• Support the development and implementation of tech transfer programs
• Create and maintain GMP documents such as risk assessments, change controls, batch records, sampling plans, and bills of materials
• Manage and update data in digital tools such as COMET SAP, MES, and DeltaV
• Plan and oversee the introduction of new programs to ensure timely execution
• Represent the tech transfer team in cross-functional project groups
• Lead small projects with moderate resource requirements and complexity
• Support the development of process descriptions, process models, and facility fit analyses for continuous and fed-batch processes
• Contribute to the design and implementation of best practices in tech transfer
• Assist in developing new solutions to enhance efficiency and minimize risks in the tech transfer process
• Analyze and optimize existing tech transfer processes based on lessons learned
• Create and maintain bills of materials (BOM), electronic batch records (gBMR, MES), and SOPs/WIs
• Apply problem-solving techniques and collaborate in interdisciplinary teams
• Foster a culture of continuous learning and process improvement
• Support knowledge management by centralizing process-related information
• Ensure compliance with safety, health, and environmental regulations
• Maintain the highest quality and compliance standards

Requirements

• University degree in a relevant scientific or technical field
• At least 5 years of experience in the pharmaceutical or biotechnology industry
• Knowledge of unit operations in monoclonal antibody manufacturing
• Basic project management skills
• Experience in creating and maintaining manufacturing-related documents (BOM, batch sheets, DeltaV)
• Proficiency in digital systems such as DeltaV, MES, eVal, SAP COMET
• Experience leading small projects with cross-functional teams
• Familiarity with cGMP regulations
• Basic understanding of the principles of tech transfer and new product introduction
• English proficiency (minimum B1), German is a plus
• Experience in a GMP-regulated environment, preferably with single-use systems
• Strong analytical and problem-solving skills in complex situations
• Experience with risk assessments and automation systems in manufacturing
• Ability to work both independently and as part of a team

Benefits at nemensis ag

• Nemensis ag is your specialized recruitment agency for Life Sciences, based in Basel
• Comprehensive consulting and support throughout the application process by our consultants
• Access to a broad client network and exciting job opportunities in Northwestern Switzerland
• Fast and straightforward placement through personalized guidance and support in the hiring process

About Us

At nemensis ag, we have connected thousands of applicants with their dream jobs, providing opportunities for career development or re-entering the job market.

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Contact: Kristina Mutidi, Consultant, Write an email

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