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CGT Raw Materials Scientist

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.

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

Job Summary: Eurofins BPT-Columbia is looking for a Scientist to join our Biologics Raw Materials team located in Columbia, Missouri. This individual will be a subject matter expert in testing Raw Materials used in Cell and Gene Therapy applications. The successful candidate will perform method establishment and validations under cGMP guidelines on a diverse set of methods including, HPLC, GC, Amino Acid Analysis, Mass Spectroscopy and FTIR. Ability to analyze data and effectively communicate results. Ability to complete work in an agreed upon timeline. Train team upon completion of method establishment and validation.

Responsibilities include (but are not limited to):

  • Designing, carrying out, and performing simple and complex experiments and procedures in accordance with all applicable regulatory (e.g. DEA, EPA, FDA, FIFRA, OECD, etc.) requirements as defined by protocol, method, and standard operating procedures (SOPs).
  • Perform method establishment and validations on a diverse set of methods including HPLC, GC, Amino Acid Analysis, Mass Spectroscopy, and FTIR.
  • Analyze data with software including Empower and effectively communicate results.
  • Train and mentor junior staff.
  • Utilize laboratory information management system (LIMS) with proficiency.
  • Is able to utilize equipment, facilities, and personnel to produce sound scientific results in a timely fashion for Eurofins clients.
  • Adheres to schedule according to Eurofins or contracting organization’s timetable and establishes daily or weekly routines necessary to ensure on-time delivery.

Qualifications

Minimum Qualifications:

  • Bachelor’s degree in chemistry, biochemistry, or biology and 5 years of experience working in a cGMP laboratory OR Master’s degree and 3 years of experience working in a cGMP laboratory OR PhD and 1+ years of experience working in a cGMP laboratory
  • Industrial experience with method establishment and cGMP validations are highly desirable
  • Authorization to work in the U.S. without restriction or sponsorship

The Ideal Candidate Would Possess:

  • Previous experience working in a CRO/CDMO adhering to cGMP regulations
  • Ability to conduct work efficiently, analyze data to ensure accuracy and report quality data.
  • Good problem solving, time management, communication, and interpersonal skills.

Additional Information

The position is full-time, Monday-Friday, 8am-4:30pm, with overtime as needed. Candidates 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 is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

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Average salary estimate

$75000 / YEARLY (est.)
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$60000K
$90000K

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What You Should Know About CGT Raw Materials Scientist, Eurofins

Join Eurofins Scientific as a CGT Raw Materials Scientist in stunning Columbia, MO! At Eurofins, a globally recognized leader in life sciences, you'll contribute to enhancing safety and sustainability in various industries through your expertise in analytical testing. In this vital role, you will focus on testing raw materials for Cell and Gene Therapy applications, ensuring they meet stringent standards. You’ll be a key player in method establishment and validations, utilizing techniques such as HPLC, GC, Amino Acid Analysis, Mass Spectroscopy, and FTIR, all while adhering strictly to cGMP guidelines. Your analytical skills will shine as you process data and communicate your findings effectively to the team. Plus, you'll have the opportunity to train and mentor junior staff, sharing your invaluable knowledge and fostering a collaborative environment. With responsibilities including conducting experiments in compliance with regulatory requirements and utilizing advanced laboratory information management systems, every day will provide new challenges and opportunities to grow. If you have a solid background in chemistry, biochemistry, or biology and prior experience in a cGMP laboratory, we would love to meet you. At Eurofins, we offer a supportive workplace culture, comprehensive benefits, and a chance to be part of a company that's making a real impact. Ready to take on this exciting role and help make life better and safer? We can't wait to hear from you!

Frequently Asked Questions (FAQs) for CGT Raw Materials Scientist Role at Eurofins
What are the main responsibilities of a CGT Raw Materials Scientist at Eurofins?

As a CGT Raw Materials Scientist at Eurofins, your main responsibilities include designing and performing experiments following regulatory standards, establishing and validating analytical methods such as HPLC and Mass Spectroscopy, and analyzing results efficiently. You'll also have the opportunity to train junior staff and ensure that all aspects of your work adhere to cGMP guidelines, contributing to the safety and efficacy of gene and cell therapies.

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What qualifications are necessary to be a CGT Raw Materials Scientist at Eurofins?

To qualify for the position of CGT Raw Materials Scientist at Eurofins, candidates should have at least a bachelor's degree in chemistry, biochemistry, or biology, with relevant experience in a cGMP laboratory. Ideally, candidates should possess 5 years of experience with a bachelor's degree or 1 year of experience with a PhD. Authorization to work in the U.S. without restrictions is also required.

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What types of analytical methods will be used by a CGT Raw Materials Scientist at Eurofins?

In the role of CGT Raw Materials Scientist at Eurofins, you will work with a variety of analytical methods. Key techniques include HPLC, GC, Amino Acid Analysis, Mass Spectroscopy, and FTIR. These tools are essential for conducting thorough method establishment and validation of raw materials essential for cell and gene therapy applications.

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What kind of environment can a CGT Raw Materials Scientist expect at Eurofins?

The environment at Eurofins for a CGT Raw Materials Scientist is dynamic and collaborative, emphasizing compliance with industry regulations and safety standards. You'll work alongside a passionate team in a full-time setting, typically Monday through Friday, 8 am to 4:30 pm, with occasional overtime. The culture at Eurofins encourages innovation, continuous learning, and professional development.

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What benefits does Eurofins offer to CGT Raw Materials Scientists?

Eurofins offers an attractive benefits package for CGT Raw Materials Scientists, including comprehensive medical coverage, dental and vision insurance, life and disability insurance, and a 401(k) plan with company matching. Employees also enjoy paid vacation and holiday time, fostering a healthy work-life balance.

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Common Interview Questions for CGT Raw Materials Scientist
Can you explain your experience with method validation in a cGMP environment?

In answering this question, highlight specific examples from your past roles where you established or validated methods, focusing on your understanding of the cGMP regulations. Discuss the processes you followed, any challenges you faced, and how you overcame them. Being specific about the techniques and tools you utilized will showcase your expertise.

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What analytical techniques are you most comfortable using, and why?

Share your proficiency with techniques such as HPLC, GC, and Mass Spectroscopy. Explain how your experience and comfort with these methods enable you to perform quality analyses effectively. Providing examples of previous projects where these techniques were employed will strengthen your response.

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How do you ensure compliance with regulatory requirements when conducting experiments?

Describe your approach to maintaining compliance, including your familiarity with relevant regulatory bodies such as the FDA and EPA. Discuss your attention to detail in preparing documentation, following SOPs, and ensuring accurate reporting. Mention any specific experiences where you succeeded in navigating regulatory challenges.

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Can you give an example of a time you had to troubleshoot an experiment?

In answering this question, share a specific incident, detailing the problem and your analytical process for troubleshooting. Explain the steps you took to identify the root cause and how you implemented a solution, showcasing your problem-solving skills and ability to adapt in the lab.

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How do you prioritize your workload in a busy laboratory setting?

Discuss your time management strategies, focusing on how you assess tasks based on urgency, importance, and potential impact. Mention tools or methodologies you may use to stay organized, such as project management software or daily checklists.

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What role do you believe communication plays in laboratory work?

Emphasize the importance of clear communication in ensuring everyone understands protocols and findings. Share how you stay open to feedback and suggestions from peers to foster a collaborative environment, ultimately leading to better outcomes in your work.

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Describe a time you mentored a junior staff member in the lab.

Provide a specific example where you supported a colleague's development. Illustrate how you approached mentoring, addressing challenges they faced, and how you helped them grow their skills. Highlight the positive impact this had on team performance.

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How do you stay current with advancements in analytical chemistry?

Discuss your commitment to professional development, including any relevant literature, conferences, or networking opportunities you engage with. Highlight specific resources, such as journals or professional organizations, that you find particularly useful to stay informed.

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What do you find most rewarding about working in a laboratory setting?

Share your passion for scientific discovery and contributing to innovative solutions that affect people's lives. Discuss specific aspects of laboratory work that motivate you, such as problem-solving, collaboration, or directly seeing the results of your work improve safety in therapies.

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Why do you want to work specifically for Eurofins as a CGT Raw Materials Scientist?

Show your enthusiasm for Eurofins by mentioning their global reputation in testing services and your admiration for their commitment to safety and sustainability. Discuss how your skills align with the mission of Eurofins and how you’re eager to contribute to impactful projects in the field of cell and gene therapy.

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Full-time, on-site
DATE POSTED
December 12, 2024

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