Downstream Process Scientist API Proteins
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

• Lead and perform downstream process development for large molecule-based products such as within the API-Proteins group.
• Leading and participating in design of experiments
• Executing the planned experiments
• Optimizing purification process steps
• Data analysis for early and late-stage products
• Lead design and execution of the development studies to identify and determine process parameter ranges for purification process steps.
• Take a lead role to transfer process from development to GMP clinical and commercial manufacturing.
• Record and analyze experimental data
• Verify data integrity and accuracy
• Report/summarize findings to the project team
• Write technical documents.

• At least a BS in a scientific related discipline
• Broad knowledge in purification process development
• Hands-on experience in one or more of the purification process development steps - cell recovery, chromatography operations, VIN, and UF/DF is required.
• Previous experience in scale-up 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