Downstream Process Scientist - Viral Vectors
Eurofins

Company Description

The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

If you're looking for a rewarding career, a place to call home, apply with us today!

Job Description

The candidate is expected to perform experiments to support downstream process development activities for viral vectors manufacturing.

• Working experience with viral vectors is required.
• Conduct purification experiments utilizing ÄktaAvant systems.
• Record and analyze experimental data, verify data integrity and accuracy.
• Report/summarize findings to the project team.
• Write technical documents and main work records in electronic notebooks.

• Bachelor's degree in life sciences or a related scientific discipline
• Authorization to work in the United States indefinitely without restriction or sponsorship
  
• Hands-on experience in purification of proteins or biologics is required.
• Broad knowledge in chromatography techniques and purification process development is required
• Previous experience with transfer of a purification process to clinical and commercial GMP manufacturing is preferred.

• Excellent full time benefits including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays