Analytical Associate Scientist - job 1 of 2

To apply for the Analytical Associate Scientist position at Eurofins, you should have a Bachelor's or Master’s degree in Biotechnology, Biochemical Engineering, Analytical Chemistry, or Chemical Engineering. Additionally, 1-3 years of relevant experience in an industrial setting is required, along with specific expertise in UV-Vis and HPLC techniques.

As an Analytical Associate Scientist at Eurofins, your main responsibilities will include providing analytical support to biotherapeutic process development teams and performing various techniques related to large molecules. This involves using UV-Vis spectroscopy and HPLC methods, alongside ensuring compliance with GMP practices and utilizing electronic laboratory notebooks.

Candidates for the Analytical Associate Scientist role should have familiarity with multiple laboratory techniques, including ultraviolet and visual light spectroscopy (UV-Vis), analytical chromatographic separations using HPLCs or UPLCs, and SEC-MALS. Having skills in small-volume multichannel pipetting and plate-based assays will also be beneficial.

Yes, the Analytical Associate Scientist position at Eurofins is a full-time role with a standard work schedule of Monday to Friday from 8:00 AM to 5:00 PM, ensuring a work-life balance while contributing to meaningful scientific advancements.

No, applicants for the Analytical Associate Scientist position at Eurofins must have the ability to work indefinitely in the United States without sponsorship. This requirement ensures that Eurofins can efficiently onboard qualified candidates.

When answering, focus on specific projects where you utilized UV-Vis spectroscopy, highlighting the techniques used and the outcomes. Emphasize your problem-solving skills and how you ensured accuracy and validity in analyses.

In your response, describe the problem you encountered, the steps you took to identify and resolve the issue, and the ultimately successful outcome. Stress your analytical thinking and adaptability under pressure.

Discuss your familiarity with GMP practices and provide specific examples of how you’ve maintained compliance in past roles, ensuring that safety and quality remain the top priority in laboratory operations.

Share a thoughtful insight into challenges you’ve faced, such as stability issues or purification complexities. Discuss how you overcame these challenges and what you learned from the experiences.

Describe your organizational system, whether it’s digital or manual, and how you handle deadlines. Mention any tools or strategies you use to maintain efficiency and accuracy in high-pressure situations.

Explain your experience with electronic lab notebooks, focusing on their benefits in data management and collaboration. Mention specific systems you are familiar with and how they enhanced your productivity and record-keeping.

Reflect on Eurofins’ reputation in the industry and express your enthusiasm for contributing to its mission. Highlight how your skills align with the company's goals and your desire to impact public health positively.

Share insights about Eurofins, emphasizing their role in biotherapeutic testing and the significance of these services in ensuring product safety and efficacy. Demonstrating knowledge of the company shows your preparedness and genuine interest.

Discuss your approach to conflict resolution, emphasizing communication and collaboration. Provide an example of a past experience where you successfully navigated a disagreement, illustrating your ability to maintain team harmony.

Highlight specific equipment you have used extensively, such as HPLC systems or pipetting technologies. Discuss the context in which you gained this experience, showcasing your hands-on skills and technical knowledge.