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Cell and Gene Therapy Scientist - job 1 of 2

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

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Average salary estimate

$100000 / YEARLY (est.)
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max
$80000K
$120000K

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 Cell and Gene Therapy Scientist, Eurofins

Are you ready to make a significant impact in the field of biotechnology? Eurofins BPT-Columbia is seeking a passionate and skilled Cell and Gene Therapy Scientist to join our dynamic Biologics Raw Materials team in Columbia, MO. In this exciting role, you will be the go-to expert in testing raw materials vital for Cell and Gene Therapy applications. Imagine being at the forefront of scientific breakthroughs while working in a supportive environment where innovation is encouraged! You’ll be conducting method validations and establishment using a diverse array of techniques like HPLC, GC, Amino Acid Analysis, Mass Spectroscopy, and FTIR—all under stringent cGMP guidelines. This role not only involves technical expertise in test procedures but also provides the opportunity to mentor junior staff and communicate vital findings effectively to ensure top-quality, safe products. Your contributions will help us maintain our reputation as leaders in the industry. If you have a comprehensive background in chemistry, biochemistry, or biology and enjoy solving problems and managing your time efficiently, we want to hear from you. At Eurofins, we offer excellent benefits, a vibrant workplace, and the chance to grow within a globally recognized company that values sustainability and safety. Come join us, and let’s innovate together!

Frequently Asked Questions (FAQs) for Cell and Gene Therapy Scientist Role at Eurofins
What are the responsibilities of a Cell and Gene Therapy Scientist at Eurofins?

As a Cell and Gene Therapy Scientist at Eurofins, your responsibilities will encompass designing and executing experiments to test raw materials for therapy applications in compliance with regulatory requirements. You will establish and validate complex methodologies, analyze results using industry-standard software, and provide training to junior team members. Your role will also involve effective communication of results and ensuring timely delivery in line with client needs.

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What qualifications are needed for the Cell and Gene Therapy Scientist position at Eurofins?

To qualify for the Cell and Gene Therapy Scientist role at Eurofins, candidates typically need a Bachelor’s degree in chemistry, biochemistry, or biology, along with significant experience in a cGMP laboratory. Alternatively, a Master’s degree with less experience or a PhD with at least one year of relevant experience is also acceptable. Familiarity with method establishment and cGMP validations is highly desirable.

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What kind of laboratory techniques will a Cell and Gene Therapy Scientist at Eurofins work with?

In the Cell and Gene Therapy Scientist position at Eurofins, you will work with various laboratory techniques, including HPLC, GC, Amino Acid Analysis, Mass Spectroscopy, and FTIR. Mastery of these techniques is crucial as they play a major role in the establishment and validation of testing methods used for raw materials in cellular therapies.

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Is there room for career growth for Cell and Gene Therapy Scientists at Eurofins?

Absolutely! Eurofins is committed to the professional development of its employees. As a Cell and Gene Therapy Scientist, you will have opportunities to advance your skills, take on more responsibilities, and potentially move into leadership positions within the company as you contribute to innovative projects and processes.

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What are the work hours for the Cell and Gene Therapy Scientist role at Eurofins?

The Cell and Gene Therapy Scientist position at Eurofins is a full-time role with standard work hours from Monday to Friday, 8 am to 4:30 pm. While overtime may be required as needed, employees enjoy a structured schedule that allows for work-life balance.

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Common Interview Questions for Cell and Gene Therapy Scientist
Can you explain your experience with method establishment in a cGMP laboratory?

In answering this question, detail specific methods you've established, emphasizing your familiarity with the protocols and regulatory guidelines. Highlight the outcomes of your method development, such as increased efficiency or accuracy, and frame your responses around how this experience will translate to success in the Cell and Gene Therapy Scientist role at Eurofins.

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

To effectively answer this question, discuss your systematic approach to compliance, referencing specific regulations like FDA and EPA standards you've worked within. Explain the importance of documentation, following SOPs, and conducting thorough reviews to ensure all procedures align with legal expectations.

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Describe a challenging project you worked on and how you managed it?

Here, you should illustrate a particular challenge you faced during a project, focusing on your problem-solving approach. Discuss the steps you took to overcome the obstacle, how you engaged with your team and resources, and the successful outcome, linking it back to your potential contributions at Eurofins.

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What techniques are you proficient in, and how will they benefit your work at Eurofins?

Highlight your expertise in techniques such as HPLC, GC, or Mass Spectroscopy. Discuss how your skills directly apply to the Cell and Gene Therapy Scientist role and how your proficiency will enhance the testing and validation processes at Eurofins.

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How do you prioritize tasks in a fast-paced laboratory environment?

Explain your time management strategies, like using task lists, prioritizing critical deadlines, and effective communication with colleagues to create a cohesive workflow. Share an example from your past experiences where these strategies led to successful project completion.

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Can you describe your experience training and mentoring junior staff?

Discuss specific instances where you've trained new employees or mentored peers, focusing on your teaching style, how you manage different learning paces, and the importance of building a strong team. This will show your leadership potential within Eurofins.

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What role does data analysis play in your experimentation process?

Clarify that data analysis is integral to verifying experimental results. Share your analytical methods and software (like Empower) you use, emphasizing how data interpretation informs future protocols and method adjustments in your line of work.

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How do you stay updated with advancements in biotechnology and regulatory changes?

Mention your proactive approach to professional development through attending workshops, reading relevant journals, or participating in industry conferences. Explain how staying informed equips you for challenges and innovations at Eurofins.

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Why do you want to work for Eurofins as a Cell and Gene Therapy Scientist?

Craft a genuine response highlighting your admiration for Eurofins’ commitment to safety and sustainability. Speak to your enthusiasm for being part of a team that leads in analytical testing and how your values align with their mission.

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What strategies do you use to communicate complex scientific findings to non-scientific stakeholders?

It's crucial to articulate complex information clearly and understandably. Discuss methods like visual aids, simplified language, and analogies. Provide examples of how you've successfully conveyed technical information in the past.

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Full-time, on-site
DATE POSTED
February 9, 2025

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