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Scientist, Data Review - job 3 of 5

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 Scientist, Data Review to join our Quality Assurance team located in Columbia, Missouri.  The Quality Assurance Associate position is 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 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, Data Review, Eurofins

If you're looking for an exciting opportunity to grow your career in the life sciences, Eurofins Scientific is thrilled to announce that we are seeking a talented Scientist, Data Review to join our Quality Assurance team in beautiful Columbia, MO. This is a fantastic role for someone who enjoys working in a laboratory environment, focusing on ensuring the accuracy and quality of scientific reports. In this position, you'll be responsible for reviewing reports under cGMP guidelines and making sure that every piece of data is precise and compliant with regulatory standards. You won't just sit at your desk—your insights and assessment will directly influence lab operations and the quality of our services. You'll collaborate closely with lab staff, conduct internal audits, and have the important task of sign-off on final reports. We welcome candidates with a background in laboratory settings or GMP pharmaceutical fields who possess strong organizational and communication skills. If you're enthusiastic, detail-oriented, and eager to contribute to making the world safer and healthier, we encourage you to apply! At Eurofins, we celebrate diversity and provide excellent benefits, including medical coverage, dental and vision options, a retirement plan with company match, and generous paid time off. Join us in making a positive impact in the life sciences sector.

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

As a Scientist, Data Review at Eurofins Scientific, your core responsibilities will include reviewing scientific reports to ensure they meet cGMP guidelines, verifying that data is accurate and complete, and maintaining high-quality documentation. You will collaborate with lab operations staff and participate in internal audits, playing a critical role in the quality assurance process.

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What qualifications are needed for the Scientist, Data Review position at Eurofins?

Candidates for the Scientist, Data Review role at Eurofins need a bachelor's degree in a relevant field such as chemistry, biology, or pharmaceutical sciences. Additionally, experience in laboratory or GMP settings, strong organizational skills, and excellent communication abilities are essential for success in this position.

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How does Eurofins ensure quality in its laboratory operations through the Scientist, Data Review?

At Eurofins, the Scientist, Data Review plays a vital role in ensuring quality by meticulously reviewing scientific reports for compliance with regulatory requirements. You will assess the integrity of the data and confirm that reports adhere to established protocols, thus maintaining Eurofins' reputation for precision and reliability in laboratory testing.

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

The work environment at Eurofins Scientific for a Scientist, Data Review is laboratory-based in Columbia, MO. You will be part of a dynamic team focusing on quality assurance, where collaboration with researchers and lab staff is essential. The role is full-time, typically from Monday to Friday, promoting a balanced and productive work atmosphere.

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What benefits does Eurofins offer for the Scientist, Data Review role?

Eurofins provides an attractive benefits package for the Scientist, Data Review position, including comprehensive medical, dental, and vision coverage, life and disability insurance, a 401(k) plan with company matching, and generous paid vacation and holidays, making it an excellent opportunity for career growth and personal well-being.

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Common Interview Questions for Scientist, Data Review
What steps do you take to ensure the quality of the scientific reports you review?

When reviewing scientific reports, I prioritize careful attention to detail. I follow a checklist based on cGMP guidelines to verify that all data meets regulatory standards. I also consult with lab staff to clarify any uncertainties and ensure comprehensive understanding of the data being reviewed.

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Describe a time when you identified a significant error in a report.

In my previous role, I discovered a crucial calculation error in a report that would have affected the final conclusions significantly. I promptly documented the issue and discussed it with my team to determine the appropriate corrective action, showcasing my commitment to quality assurance.

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How do you handle tight deadlines when reviewing data?

I effectively prioritize my tasks by breaking down the review process into manageable sections and setting milestones. This method allows me to maintain quality while working efficiently, ensuring that I meet deadlines without compromising accuracy or thoroughness.

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What tools or software are you familiar with in a laboratory environment?

In my experience, I have utilized a variety of laboratory information management systems (LIMS) for data tracking and report generation, as well as statistical analysis software to evaluate data. I am always eager to learn new tools that enhance efficiency in the review process.

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How do you ensure compliance with both company policies and regulatory standards?

Compliance starts with a strong understanding of both internal policies and external regulations. I regularly review guidelines and attend training sessions. I also ensure that I apply this knowledge consistently in my daily work and maintain transparent communication with my supervisors.

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What is your approach to conducting internal audits?

My approach to internal audits involves thorough preparation and collaboration with team members. I create a detailed plan that outlines key areas to evaluate, and I engage team members in discussions to gather insights, ensuring a comprehensive audit process that identifies possible areas for improvement.

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Can you provide an example of how you efficiently solved a problem during a report review?

During a report review, I encountered discrepancies in data sets. To resolve this, I organized a quick meeting with the research team to clarify procedures and ensure all data sources were re-verified. This not only solved the issue but also fostered better communication for future reviews.

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How do you manage conflicts in a team setting?

I manage conflicts by listening to all perspectives without bias and facilitating an open discussion to uncover the root cause. I believe in finding common ground and focusing on the goals we share as a team, which fosters a collaborative atmosphere.

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What motivates you to work in the field of quality assurance?

I am motivated by the importance of producing reliable and scientifically sound results. Being part of a process that ensures public safety and contributes positively to society drives me. I find fulfillment in knowing my work as a Scientist, Data Review at Eurofins can lead to impactful outcomes.

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Why do you want to work at Eurofins Scientific?

I am impressed by Eurofins Scientific's commitment to quality and its leadership in analytical testing. I admire the company's focus on making the world safer and healthier, and I want to contribute my skills to a team that aligns with my passion for impactful scientific work.

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DATE POSTED
April 21, 2025

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