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Scientist I - job 1 of 3

Company Description

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 is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

Job Description

Position Summary:

The Scientist I performs testing activities as directed by Specialty Analysis Manager or Lab Director  in accordance with all applicable company and regulatory guidelines and designs experiments, operates instruments, assists other chemists, collects and interprets data, writes but also peer reviews data and/or reports especially for challenging, non-routine investigations, custom method development, method validation, GLP Study work, product testing/development work. 

Authority:

The Scientist receives sufficient authority from, and is accountable to, the Specialty Analysis Manager or Lab Director, or appointed designate, for the successful completion of assigned duties and responsibilities and has the authority to take action necessary to carry out the duties and responsibilities of this position and to identify the occurrence of departures from the quality system or from the procedures for performing tests and/or calibrations, so long as such action does not deviate from established company guidelines, is consistent with sound technical and business judgment, and follows the practices of the laboratory.

Essential Duties and Responsibilities:

  1. Perform testing activities as directed by Specialty Analysis Manager or Lab Director in accordance with all applicable company and regulatory guidelines.
  2. Wet chemistry techniques utilized will include but are not limited to gravimetry, titrimetry, colorimetry and others as needed including sample preparation, isolations, filtrations, extractions.
  3. Instrumentation utilized will include a wide array including not limited to HPLC, LCMS, GCFID/ECD, GCMS, ICP-OES, ICP-MS, AA, IC, and other instruments and techniques as needed to meet customer expectations (includes outsourcing selective testing when appropriate).
  4. Perform and document method transfers, development work, validations/verifications.
  5. Maintain neat and accurate records.
  6. Ensuring that the client receives quality data by compiling and/or reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations or other internationally recognized standards (e.g., ISO/IEC 17025:2017).
  7. Interact with clients to assist in selection of test methods and interpretation of test data.  Assist Sales and Business Team members on quote review if requested.
  8. Design custom projects or studies, and offer interpretation, custom reports or consultation on test data.
  9. Enter testing data into LIMS and monitor for QC failures.
  10. Assist lab staff in determining corrective actions for QC failures.
  11. Review and approve laboratory analytical data including peer review
  12. Review and issue reports to clients.
  13. Maintain chemical/reagent traceability.
  14. Support the maintenance of controlled documents related to laboratory operations/testing through editing of documents and/or reviewing revisions.
  15. Support quality system improvements through completion of Corrective and Preventive Action forms, documenting Non-Conformances and Client Complaints, and assisting with internal audit findings as assigned by Quality Manager.
  16. Maintain regular attendance and punctuality
  17. Conducts all activities in a safe and efficient manner
  18. Performs other duties as assigned
  19. Assist with case studies, white papers if requested by Sr. Management for marketing purposes.
  20. Attend industry-appropriate symposia, training, webinars, journals to remain current on analytical techniques, new developments.

Qualifications

  • BS or greater in Chemistry or related field, 2+ years experience in a commercial laboratory in an autonomous environment
  • Proficiency at HPLC, LCMS, GC, GCMS, and knowledge of all other major analytical instrument capabilities is imperative
  • Knowledge of ISO 17025, CVM, FDA or other regulatory standards

Additional Information

Schedule:

  • Monday-Friday 9:00am-5:00pm

What we offer:

  • 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

Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

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Average salary estimate

$70000 / YEARLY (est.)
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$60000K
$80000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About Scientist I, Eurofins

Are you ready to make an impact in the world of science? Join Eurofins Scientific as a Scientist I in New Berlin, WI, and be part of a global leader that ensures safety and authenticity in food, pharmaceuticals, and environmental testing! In this role, you'll dive into testing activities that contribute to the high standards Eurofins upholds. Whether it’s performing wet chemistry techniques or operating a variety of analytical instruments such as HPLC and GCMS, no two days will be the same. You'll be designing experiments and collaborating with your fellow scientists to collect and interpret data, while also getting the chance to review reports for accuracy and clarity. You'll interact with clients to help them select the best test methods and interpret the resulting data, making your contributions essential to their success. We've got your back too; with generous benefits, including comprehensive health coverage and a 401(k) plan with a company match, Eurofins values your hard work. Plus, you’ll have the opportunity for ongoing learning and professional growth as you attend industry events and webinars. If you have a BS in Chemistry or a related field and a minimum of two years of experience in a commercial laboratory, we can’t wait to have you on board. Come be part of our mission to make life safer and healthier, one test at a time!

Frequently Asked Questions (FAQs) for Scientist I Role at Eurofins
What are the primary responsibilities of a Scientist I at Eurofins Scientific?

The Scientist I at Eurofins Scientific is responsible for performing various testing activities as directed by the Specialty Analysis Manager or Lab Director. This includes designing and executing experiments, operating analytical instruments, and interpreting data while ensuring compliance with all company and regulatory guidelines. You’ll engage in intricate processes such as method validation, quality control, and client consultations to guarantee top-notch service.

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What qualifications are required for the Scientist I position at Eurofins Scientific?

To qualify as a Scientist I at Eurofins Scientific, candidates must hold a Bachelor's degree or higher in Chemistry or a related field, alongside at least 2 years of experience working in a commercial laboratory. Proficiency in operating analytical instruments like HPLC and GCMS is essential, along with a solid understanding of ISO 17025 regulatory standards.

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What types of analytical instruments will I work with as a Scientist I at Eurofins Scientific?

In the Scientist I role at Eurofins Scientific, you’ll work with a diverse range of analytical instruments, including but not limited to HPLC, LCMS, GCMS, ICP-MS, and AA. Mastery of these tools is essential for carrying out your duties effectively and ensuring the quality of the data produced.

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What does a typical day look like for a Scientist I at Eurofins Scientific?

A typical day for a Scientist I at Eurofins Scientific involves performing a variety of testing activities, collaborating with colleagues, and interacting with clients. You’ll document methods, validate procedures, and enter data into the Laboratory Information Management System (LIMS). Regular participation in team meetings and ongoing learning through industry events is also part of your daily routine.

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What kind of career development opportunities are available for Scientist Is at Eurofins Scientific?

Eurofins Scientific emphasizes your professional growth by providing various career development opportunities. As a Scientist I, you'll have access to training sessions, industry-specific webinars, and chances to attend symposia to enhance your skills and knowledge. Additionally, Eurofins supports your pursuit of advanced roles as you gain experience and contribute value to the company.

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Common Interview Questions for Scientist I
How do you ensure accuracy and precision in your testing procedures?

In answering this question, highlight your attention to detail and your experience with protocols that guarantee data integrity. Discuss your familiarity with quality control measures and your proactive approach to identifying and rectifying issues during experiments.

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Can you describe your experience with HPLC and its applications?

When responding, detail your practical experience with HPLC analysis and any specific projects that illustrate your proficiency. Highlight your understanding of method development and optimization, as well as your ability to troubleshoot when challenges arise.

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What is your approach to writing and peer-reviewing technical reports?

Explain the importance of clarity and thoroughness in your reports to ensure they meet the expectations of both regulatory standards and client needs. Share your process for reviewing other scientists' work and how you provide constructive feedback.

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How do you handle working on multiple projects simultaneously?

For this question, emphasize your organizational skills and time management strategies. Discuss how you prioritize tasks based on deadlines and project importance, as well as any specific tools or methods you use to keep track of progress.

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Can you give an example of a challenging investigation you’ve conducted?

Share a specific scenario where you faced a significant challenge, focusing on your analytical thinking and problem-solving skills. Describe the approach you took and the successful outcome that resulted from your efforts.

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How do you stay updated with current scientific trends and advancements?

Mention the various resources you utilize, such as scientific journals, webinars, and industry conferences. This demonstrates your commitment to continuous learning and growth within your field and how that benefits your role as a Scientist I.

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What strategies do you use for effective collaboration with team members?

Discuss your communication style and how you tailor interactions based on team dynamics. Provide examples of successful collaborations that led to improved processes or outcomes and highlight the importance of teamwork in a laboratory setting.

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What is your understanding of GLP and its significance in laboratory testing?

Your answer should reflect a solid understanding of Good Laboratory Practices (GLP) and their importance in guaranteeing the reliability and integrity of the testing process. Provide examples of how you ensure adherence to GLP in your daily activities.

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How do you approach method development and validation?

In your response, demonstrate your systematic approach to designing experiments, including identifying objectives, selecting methods, and validating results. Highlight any relevant experiences that showcase your technical expertise in this area.

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What role does client communication play in your position as a Scientist I?

Explain that effective client communication is crucial for understanding their needs and ensuring satisfaction. Discuss your experience interacting with clients, assisting with method selections, and interpreting test data while maintaining professionalism and clarity.

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DATE POSTED
April 17, 2025

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