Associate Scientist, R&D Pathogen Safety

Associate Scientist, R&D Pathogen Safety

Eurofins

Bern, Switzerland

Job Description

As an Associate Scientist in the R&D Pathogen Safety team, you will play a key role in contributing to virus validation studies and developing virus elimination steps in manufacturing processes. You will assist in designing experimental study plans, conduct and analyze experimental work, and document and communicate results to the manager and project team. Your responsibilities will also include maintaining biological systems, performing viral titrations, and assisting with technical documentation and equipment procurement.

Responsibilities

• Contribute to virus validation studies and develop virus elimination steps in manufacturing processes
• Assist in designing experimental study plans in consultation with the supervisor
• Assist with authorship/review of (GLP) study documentation, including protocols and reports
• Plan and conduct experimental work, analyze data, and communicate results in reports or presentations
• Control and maintain biological systems, including cell culture work, virus, and cell strain maintenance
• Perform viral titrations to determine viral titers under L2/S2 (and L3/S3) conditions
• Conduct various analytical methods, such as protein determinations and pH measurements
• Operate complex instruments and process/prep raw data
• Collect, prepare, and distribute samples/data in coordination with other departments
• Participate in local and global projects
• Create and maintain records within internal documentation systems
• Create and revise technical documents, including operating procedures, test/process protocols, and reports
• Assist in the procurement of new equipment and systems
• Maintain laboratory equipment according to specific quality standards (e.g., GLP)
• Coordinate availability of materials, solutions, and reagents

Qualifications

• Bachelor's or Master's degree in scientific studies
• Proficient use of MS Office
• Preparation of scientific reports. Documentation of scientific reports
• Knowledge of cell culture and virological work
• GxP knowledge
• Work experience is an advantage, preferably with cell culture work or microbiological/virological experience. Work experience in the pharmaceutical industry, preferably biotherapeutics or plasma proteins
• Experience with handling L2 (and L3) viruses
• Experience in virus titration (TCID50)

Key Competencies

• Ability to independently plan, execute, and evaluate laboratory experiments
• Excellent communication skills with a proactive and positive working attitude
• Action-oriented with a sense of urgency to complete tasks
• Willingness to take responsibility in laboratory organization and manage time for multiple experiments
• Flexibility in daily work and adaptability to organizational changes
• Strong team player with an understanding of customer needs
• Demonstrates integrity, honesty, and willingness to adhere to safety, quality, and company policies
• Cross-cultural sensitivity and flexibility, respecting differences in people and cultures
• Willingness to supervise apprentice technicians

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