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Scientist, Data Review - job 2 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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It 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. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer 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

*THIS IS NOT A DATA SCIENCE POSITION*

Eurofins BPT-Columbia is looking for a Associate Scientist, Data Review to join our Quality Assurance team located in Columbia, Missouri.  The Quality Assurance Associate position is an entry-level position involved in day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). 

  • Review scientific reports under cGMP guidelines to ensure regulatory requirements have been met, the data is whole and accurate, and the report is of high quality.
  • Assisting with internal audits
  • Work closely with lab operations staff on a day-to-day basis and have the authority and responsibility for final report sign-off.
  • Other duties as assigned.

Qualifications

The ideal candidate would possess:

  • Experience in a laboratory setting or GMP pharmaceutical setting.
  • Good organizational skills; ability to follow direction and good communication skills are required.
  • Strong computer, scientific, and organizational skills.
  • Excellent communication (oral and written) and attention to detail.
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude.
  • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.

Minimum Qualifications

  • Bachelor’s degree in relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field or degree with comparable coursework in the above areas.
  • Authorization to work in the United States indefinitely without restriction or sponsorship.

Additional Information

Position is full-time position, Monday - Friday 8:00am - 4:30pm. Candidates currently living within a commutable distance of Columbia, MO are encouraged to apply.

  • 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

To learn more about Eurofins, please explore our website www.eurofinsus.com.

Eurofins USA BioPharma Services is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

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Average salary estimate

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

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What You Should Know About Scientist, Data Review, Eurofins

Are you ready to dive into the world of scientific innovation? Eurofins Scientific is on the lookout for a passionate Scientist, Data Review to join our dynamic Quality Assurance team in Columbia, Missouri. This isn't just another job; it's an opportunity to be part of a global leader in analytical testing! As a Scientist in this entry-level position, you will play a critical role in ensuring that our scientific reports meet strict cGMP guidelines and regulatory requirements, making certain the data is accurate and of exceptional quality. Your daily activities will involve collaborating closely with laboratory operations staff, assisting with internal audits, and utilizing your keen attention to detail for report sign-offs. If you thrive in a fast-paced lab environment, this role allows you to learn new techniques while honing your skills and making meaningful contributions to projects that promote health and safety. We're looking for someone with a Bachelor’s degree in fields like chemistry, biochemistry, or biology. If you have experience in a laboratory or GMP setting, great organizational skills, and a positive, self-motivated attitude, we want to hear from you! Join us at Eurofins, where the science isn't just about data—it's about making a difference in people’s lives. Come help us ensure safety, authenticity, and purity in the products that matter most to you and your community!

Frequently Asked Questions (FAQs) for Scientist, Data Review Role at Eurofins
What are the responsibilities of a Scientist, Data Review at Eurofins?

As a Scientist, Data Review at Eurofins, your primary responsibilities include reviewing scientific reports to ensure they comply with cGMP guidelines, assisting with internal audits, and collaborating closely with lab operations staff. You will have the authority to sign off on final reports, ensuring that the data is both accurate and of the highest quality.

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What qualifications are necessary for the Scientist, Data Review role at Eurofins?

To qualify for the Scientist, Data Review position at Eurofins, candidates must possess a Bachelor’s degree in related fields such as chemistry, biochemistry, biology, or chemical engineering. Additionally, prior experience in a laboratory or GMP setting, along with strong communication and organizational skills, is highly advantageous.

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What work environment can a Scientist, Data Review expect at Eurofins?

At Eurofins, the Scientist, Data Review will work in a bustling laboratory environment where collaboration and attention to detail are key. The lab operates under strict standard operating procedures, providing a structured yet dynamic space that encourages scientific exploration and innovation.

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Is the Scientist, Data Review position at Eurofins a full-time role?

Yes, the Scientist, Data Review position at Eurofins is a full-time role, usually operating from Monday to Friday, 8:00 AM to 4:30 PM. This schedule ensures you have a balanced work-life while contributing to significant scientific projects.

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What benefits does Eurofins offer to its Scientist, Data Review team members?

Eurofins offers a comprehensive benefits package for the Scientist, Data Review position, including medical coverage, dental and vision options, life and disability insurance, a 401(k) plan with company match, as well as paid vacation and holidays, promoting a healthy work-life balance.

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Common Interview Questions for Scientist, Data Review
Can you describe your experience in a laboratory setting relevant to the Scientist, Data Review role?

When answering this question, focus on specific experiences you've had in laboratory work, emphasizing your familiarity with protocols, standard operating procedures, and any direct experience related to data review. Highlight your attention to detail and organization as it pertains to quality assurance.

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What is your understanding of cGMP guidelines and their importance in scientific research?

In your response, explain that cGMP stands for current Good Manufacturing Practice, which ensures that products are consistently produced and controlled according to quality standards. Discuss how adherence to these guidelines is critical in the lab setting to ensure drug safety and effectiveness.

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How do you prioritize tasks when working on multiple projects simultaneously?

Share your strategies for effective time management, such as creating priority lists, setting deadlines, and utilizing productivity tools. Provide examples of how you've managed multiple responsibilities while maintaining quality in your work.

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Can you give an example of a time you identified an error in laboratory data? How did you handle it?

Use the STAR method (Situation, Task, Action, Result) to explain a specific situation where you caught an error. Detail the steps you took to investigate the issue and ensure accurate reporting, showcasing your problem-solving and analytical skills.

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How do you ensure clear communication within a team in a lab environment?

Discuss your approach to communication, such as regular team meetings, status updates, and using collaborative tools. Emphasize the importance of clear directions and constructive feedback to maintain team alignment and promote a positive working environment.

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What motivates you to work in a Quality Assurance role?

Express your passion for ensuring quality in scientific research and products. Talk about how this aligns with your personal values, and the satisfaction you derive from making a positive impact on health and safety through your work.

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Describe how you handle constructive criticism.

Explain that you see constructive criticism as an opportunity for growth. Provide an example of a situation where you received feedback, how you acted upon it, and the improvements you made as a result.

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What specific computer skills do you bring to the Scientist, Data Review position?

Outline your proficiency with laboratory software, data management systems, and any statistical analysis tools. Discuss how these skills enhance your ability to conduct thorough data reviews and ensure compliance with regulatory standards.

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What is your approach to maintaining accurate records in a laboratory?

Share your methods for ensuring accuracy, such as meticulous documentation practices, regular reviews of lab notebooks, and double-checking data entries. Highlight your understanding of compliance standards and their importance in scientific integrity.

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Why do you think teamwork is important in scientific research?

Emphasize your belief that teamwork fosters diverse perspectives, enhances creativity, and improves problem-solving. Discuss examples of successful collaborations you've been part of and how they led to better outcomes in research projects.

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DATE POSTED
April 5, 2025

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