Job Description
As a Scientist in the R&D Pathogen Safety team, you will play a critical role in designing and conducting virus validation studies and developing virus elimination steps in manufacturing processes. Your responsibilities will include developing experimental study designs, guiding study personnel, preparing GLP study documentation, conducting experimental work, and analyzing and communicating results. Additionally, you will maintain biological systems, perform viral titrations, and use various analytical methods. You will also create technical documents, participate in projects, and maintain records within internal documentation systems.
Responsibilities
1. Design and conduct virus validation studies and develop virus elimination steps in manufacturing processes
2. Develop experimental study designs in consultation with the supervisor
3. Guide study personnel in conducting virus validation studies
4. Prepare (GLP) study documentation, including protocols and reports
5. Plan and conduct experimental work, analyze data, and communicate results in reports or presentations
6. Control and maintain biological systems, including cell culture work, virus, and cell strain maintenance
7. Perform viral titrations to determine viral titers under L2/S2 (and L3/S3) conditions
8. Conduct various analytical methods, such as protein determinations and pH measurements
9. Operate complex instruments and process/prep raw data
10. Collect, prepare, and distribute samples/data in coordination with other departments
11. Participate in local and global projects
12. Create and maintain records within internal documentation systems
13. Create and revise technical documents, including operating procedures, test/process protocols, and reports
14. Assist in the procurement of new equipment and systems
15. Maintain laboratory equipment according to specific quality standards (e.g., GLP)
16. Coordinate availability of materials, solutions, and reagents
Qualifications
1. Master's degree or doctorate in scientific studies
2. Proficient use of MS Office
3. Practical performance of complex laboratory experiments using protein purification methods
4. Preparation of scientific reports
5. Documentation of scientific studies
6. Knowledge of cell culture and virological work
7. GxP knowledge
8. Work experience is an advantage, preferably with cell culture work or microbiological/virological experience. In the pharmaceutical industry, preferably biotherapeutics or plasma proteins
9. Experience with handling RG2 (and RG3) viruses
10. Experience in virus titration (TCID50)
Company Culture
At Eurofins PSS, our company culture is deeply rooted in our four core values: Teamwork, Integrity, Superlative Customer Satisfaction, and Productivity. We believe in fostering a collaborative environment where every team member is encouraged to contribute their unique expertise and ideas. Our commitment to integrity drives us to uphold the highest ethical standards in all our endeavors. We strive for superlative customer satisfaction by understanding and exceeding our clients' expectations. Embracing productivity, we continuously seek innovative ways to streamline processes and deliver exceptional results. Together, these values form the foundation of a supportive and empowering workplace, enabling us to achieve excellence in everything we do.
Opportunities For Growth
As part of our commitment to employee development, we offer abundant growth opportunities at Eurofins PSS. You'll have access to learning and development programs, coaching & mentorship, and the chance to take on challenging projects, empowering you to achieve your professional aspirations.
Equal Opportunity Employer Statement
At Eurofins PSS, we are dedicated to being an equal opportunity employer, embracing diversity, and cultivating an inclusive workplace where every individual's unique background and perspective are valued, respected, and celebrated.
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