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Scientist, Data Review

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

$60000 / YEARLY (est.)
min
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$50000K
$70000K

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 to kickstart your career in a rewarding and dynamic environment, Eurofins Scientific is excited to offer a position as a Scientist, Data Review in Columbia, MO! This entry-level role in our Quality Assurance team will allow you to dive into the fascinating world of analytical testing services. Here at Eurofins, we ensure the safety and quality of food, water, pharmaceuticals, and more, making a tangible impact on people's lives. As a Scientist focused on data review, you'll take on essential responsibilities like reviewing scientific reports following cGMP guidelines to verify data accuracy and ensure quality standards are met. Collaboration is key, and you'll work closely with lab operations staff, with the authority to sign off on final reports. Every day presents a new opportunity to assist with internal audits and refine your skills in a laboratory setting. We're looking for someone with a keen eye for detail, excellent communication skills, and a positive attitude to learn and grow with us. If you have a Bachelor's degree in a relevant field and some experience in laboratory or GMP settings, we want to hear from you! Join Eurofins and be part of a global leader dedicated to making life safer and healthier for everyone.

Frequently Asked Questions (FAQs) for Scientist, Data Review Role at Eurofins
What responsibilities does the Scientist, Data Review at Eurofins entail?

As a Scientist, Data Review at Eurofins, you will be responsible for reviewing scientific reports to ensure they comply with cGMP guidelines, confirming the accuracy of data and maintaining high-quality reports. Key duties include assisting with internal audits and collaborating with lab operations staff, granting you the authority to sign off on final reports effectively.

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

To qualify for the Scientist, Data Review role at Eurofins, candidates must hold a Bachelor's degree in a relevant discipline such as chemistry, biochemistry, or biology. Additionally, experience in a laboratory setting or GMP pharmaceuticals is valued, alongside strong organizational skills and the ability to communicate effectively.

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What is the work schedule for Eurofins' Scientist, Data Review position?

The Scientist, Data Review position at Eurofins is a full-time role, requiring a Monday through Friday work schedule from 8:00 AM to 4:30 PM. This fixed schedule allows for a balanced work-life routine while engaging in rewarding scientific responsibilities.

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How does Eurofins support career growth for Scientists in Data Review?

Eurofins is dedicated to fostering a culture of learning and development. As a Scientist in Data Review, you will have opportunities to learn new techniques and collaborate closely with experienced professionals. This exposure will not only enhance your skills but may also lead to further career progression within the Eurofins network.

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What benefits does Eurofins offer to their Scientist, Data Review employees?

Employees in the Scientist, Data Review position at Eurofins enjoy a comprehensive benefits package that includes medical, dental, and vision coverage, life and disability insurance, a 401(k) plan with company match, as well as paid vacation and holidays, creating a supportive and secure work environment.

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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, highlight any relevant laboratory experience, emphasizing your understanding of data review processes and cGMP regulations. Discuss specific tasks you've handled and how they relate to the quality assurance role.

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What steps do you take to ensure accuracy in your reports?

In your response, outline systematic methods you use to review and verify data accuracy, such as double-checking calculations, understanding protocols, and asking for clarification when necessary. Stress the importance of detail-oriented work in a quality assurance context.

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How do you handle tight deadlines while ensuring quality work?

Discuss how you prioritize tasks, manage your time efficiently, and maintain a high standard of quality even under pressure. Share specific examples from past experiences that showcase your skills in managing deadlines while producing quality outcomes.

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What approaches do you use for effective communication in a team?

Outline your strategies for effective communication, such as active listening, providing constructive feedback, and maintaining transparency with your coworkers. Emphasize the importance of teamwork in achieving quality assurance goals.

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Describe a time when you identified an error in data or reports.

When responding, share a specific scenario where you successfully identified an error, explain the steps you took to address it, and emphasize the importance of accuracy in maintaining quality. This demonstrates your critical thinking and problem-solving skills.

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

Here, show your passion for ensuring safety and compliance in scientific work. Discuss how you find fulfillment in contributing to public health and safety through quality assurance processes and how working at Eurofins aligns with your values.

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Can you walk us through the cGMP guidelines and their significance?

In your answer, define cGMP (current Good Manufacturing Practices) and explain their importance in maintaining product quality and regulatory compliance in laboratories. Highlight knowledge you have about these practices and their impact on overall safety.

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How do you adapt to new procedures in a lab environment?

Discuss your willingness to learn and adapt to new protocols. Provide an example of a time when you successfully embraced a new procedure and how that improved your performance within the laboratory setting.

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What are your long-term career goals in quality assurance?

Articulate your aspirations within the field of quality assurance, stressing your commitment to professional growth. Discuss potential certifications or advancements you seek to achieve and how you see yourself evolving within the Eurofins organization.

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What role does attention to detail play in quality assurance?

In your response, emphasize the critical role attention to detail plays in ensuring data accuracy and regulatory compliance. Share an example of how meticulous attention has directly contributed to successful outcomes in your previous roles.

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Full-time, on-site
DATE POSTED
March 18, 2025

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