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 schedule for this role is 1st shift, Tuesday-Saturday

• Perform Upstream process development utilizing the FlatBUGsystems for large molecule based products


• Perform duties in a protocol-driven work, such as cell culture, and running 5L bioreactors


• Supporting lab work associated with development and scale-up projects within the API-Proteins area


• Responsible for organizing records, capturing results into data sheets, and contributing to technical reports in a team environment as well as contributing individually to meet project timeline and objectives.


• Assist with general lab upkeep and organization efforts, which includes decontamination and disposal of large-scale cell culture/bioreactor wastes


• Conduct, analysis and reporting of data in accordance with requirements set forth by the department.


• Record experimental data and accurate and highly organized laboratory notebooks.

• Broad knowledge in upstream process development and hands-on experience is desired.


• Bachelors or Master's degree in biopharmaceutical, biotechnology or pharmaceutical disciplinerequired

• 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