Scientist I - job 1 of 2

As a Scientist I at Eurofins, your main responsibilities include independently operating analytical instruments such as HPLC, GC, and MS, preparing samples for testing, and setting up new analytical processes. You will also be responsible for method validation and executing transfer protocols, all while ensuring compliance with GMP documentation standards.

To qualify for the Scientist I position at Eurofins, you need a BS in chemistry, analytical chemistry, biochemistry, or a related field. A minimum of one year of experience in analytical testing within a cGMP environment is necessary. Additionally, candidates must have the ability to work in the U.S. without any restrictions or sponsorship.

Key skills for the Scientist I role at Eurofins include strong communication (both written and oral), proficiency in various analytical techniques, and organizational abilities. The ideal candidate should also be able to multitask, follow instructions accurately, and adhere to company policies while maintaining precise records.

The Scientist I position at Eurofins offers a full-time schedule, Monday through Friday, from 8 am to 4 pm, with additional overtime as needed to manage project demands and responsiveness to testing requirements.

As a Scientist I at Eurofins, you can look forward to excellent benefits including comprehensive medical, dental, and vision coverage, life and disability insurance, a 401(k) plan with company matching, and paid time off for vacations and holidays, making it an attractive opportunity for career growth.

In interviews, discuss your hands-on experience with HPLC, emphasizing the importance of calibration, quality controls, and data integrity. Share a specific example where you identified an anomaly in test results and how you rectified it, showcasing your analytical skills.

For this question, reflect on an actual incident where you faced compliance or procedural difficulties. Outline the challenge, your approach, and the solutions you implemented, demonstrating your ability to maintain GMP standards while being detail-oriented.

Identify the techniques you have significant experience with, such as GC, MS, or other forms of chemical analysis. Provide examples of how you have applied these techniques effectively in past roles to demonstrate your hands-on expertise.

Discuss your time management strategies, including how you assess project urgency, set deadlines, and adjust your priorities as necessary. Give examples of how you successfully managed overlapping deadlines in a past position.

Highlight the critical aspects of GMP documentation you adhere to, such as maintaining accuracy and thoroughness in your records. Describe a systematic approach you employ to stay compliant, including methods of reviewing and verifying your documentation before submission.

Outline the sample preparation process you follow, emphasizing accuracy and consistency. Discuss any particular protocols or methods you've developed or optimized to ensure high-quality sample preparation in past roles.

Express your commitment to continuous learning through professional workshops, webinars, and scientific journals. Mention specific resources or groups that have helped you stay informed about industry trends and technological advancements.

Articulate that attention to detail, along with curiosity and problem-solving skills, are crucial qualities. Provide examples from your experience that show how these traits positively impacted your work in method development or validation.

Describe your systematic approach to troubleshooting, starting from isolating the issue, checking calibration, and reviewing maintenance logs. Provide a case study where your troubleshooting led to resolving an instrument failure effectively.

Share your passion for contributing to healthcare advancements and mention any specific incidents that inspired you to pursue a career in analytical chemistry. Most importantly, connect this motivation to how your role as a Scientist I at Eurofins makes a difference in people's lives.