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Bioassay Analyst

Company Description

The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.

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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

If you’re looking for a rewarding career, apply with us today!  

Job Description

Responsibilities:

  • Develop, optimize, and qualify analytical methods for biological therapeutic product release and characterization testing in a compliance-based environment.
  • Conduct method development, qualification, and process support work, including protocol/report documentation and presentations.
  • Perform analytical testing, including liquid chromatography and plate-based assays.
  • Execute method development for elucidating and monitoring functional properties of protein therapeutics and quantifying process- and product-related impurities.
  • Participate in technology transfer activities, regulatory support, and project teams as needed.

Qualifications

Qualifications:

  • BS in Cell and Molecular Biology, Biochemistry, or Pharmaceutical concentration with 2 years of cell-based assay experience, or MS in related field with 6 months of experience
  • Proficiency in cell culture and immunological methods (e.g., Bioassay, ELISA, Octet protein binding assays)
  • Experience with high throughput technologies and automated liquid handling systems
  • Familiarity with GMP/GLP environment
  • Strong analytical and problem-solving skills with ability to work independently and in teams
  • Excellent communication skills and attention to detail
  • Authorization to work in the United States indefinitely without restriction or sponsorship

Additional Information

What to Expect in the Hiring Process: 

  • 10-15 Minute Phone Interview with the Region Recruiter
  • 45-60 Minute Virtual Interview with the Manager and/or Group Leader
  • 30 Minute Virtual Meeting with the Site Director 

Additional Details: 

The position is full-time, Monday-Friday from 8 am-5 pm. Candidates living within a commutable distance of Lexington, Massachusettes, and the surrounding areas 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 holiday

Eurofins Lancaster Laboratories Professional Scientific Services® (PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.

We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.

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

 

Eurofins USA PSS Insourcing Solutions 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

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What You Should Know About Bioassay Analyst , Eurofins

If you're passionate about cutting-edge scientific processes and want to make a significant impact in the biopharmaceutical industry, then the Bioassay Analyst position at Eurofins in Lexington, MA, could be the perfect fit for you! At Eurofins, we recognize that the work we do not only matters but so do our employees. We’re dedicated to your professional growth, offering the opportunity to advance your career from the ground up. As a Bioassay Analyst, you will be developing, optimizing, and qualifying analytical methods tailored to biological therapeutic product release and characterization testing, all in a compliance-centric environment. Your day-to-day responsibilities will include elucidating functional properties of protein therapeutics and performing method development to ensure the highest quality standards are met. Here, you’ll collaborate with a dynamic team to conduct analytical testing utilizing techniques like liquid chromatography and plate-based assays. The environment at Eurofins encourages both independent problem-solving and teamwork, fostering excellent communication skills among our analysts. If you meet our qualifications and are eager to join a company that promotes work-life balance while offering a competitive benefits package, we encourage you to apply today!

Frequently Asked Questions (FAQs) for Bioassay Analyst Role at Eurofins
What are the key responsibilities of a Bioassay Analyst at Eurofins?

As a Bioassay Analyst at Eurofins, your primary responsibilities will include developing, optimizing, and qualifying analytical methods for biological therapeutic product testing, conducting protocol documentation, performing analytical testing, and collaborating on regulatory support efforts within project teams.

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What qualifications do I need to apply for the Bioassay Analyst position at Eurofins?

To apply for the Bioassay Analyst position at Eurofins, you should have a BS in Cell and Molecular Biology, Biochemistry, or a related field with at least two years of cell-based assay experience, or an MS degree with six months of relevant experience. Proficiency in cell culture, immunological methods, and familiarity with GMP/GLP environments is essential.

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What kind of testing methods will I use as a Bioassay Analyst at Eurofins?

As a Bioassay Analyst at Eurofins, you will utilize various analytical testing methods, with a strong emphasis on liquid chromatography and plate-based assays. You'll also participate in high throughput techniques and automated liquid handling systems to ensure the efficient and accurate testing of therapeutic products.

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What skills are important for a successful Bioassay Analyst at Eurofins?

Successful Bioassay Analysts at Eurofins possess strong analytical and problem-solving skills, attention to detail, and the ability to work both independently and in teams. Excellent communication skills are necessary for effective collaboration and ensuring compliance in all laboratory processes.

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What does the hiring process look like for a Bioassay Analyst at Eurofins?

The hiring process for a Bioassay Analyst at Eurofins involves a brief phone interview with the Recruiter, followed by a virtual interview with the Manager or Group Leader and a final virtual meeting with the Site Director. This comprehensive approach helps ensure the best fit for both the candidate and the company.

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Common Interview Questions for Bioassay Analyst
Can you describe your experience with cell-based assays relevant to the Bioassay Analyst role?

When discussing your experience with cell-based assays, focus on specific techniques you've used, like ELISA or Octet assays. Provide examples of how you developed these assays and the role they played in your previous projects, demonstrating your ability to operate in a compliance-centric environment.

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How do you approach method development for biological assays?

Explain your systematic approach to method development, emphasizing the importance of understanding the therapeutic product, defining the assay's objectives, optimizing variables, and ensuring thorough documentation. Highlight the necessity of adhering to industry regulations throughout this process.

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What challenges have you faced in a GMP or GLP environment?

Discuss specific challenges you have encountered in GMP or GLP settings, such as maintaining accurate records, dealing with equipment malfunctions, or addressing unexpected results. Be sure to mention how you addressed these challenges, focusing on how you ensured quality and compliance.

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Can you give an example of a project where you worked in a team setting?

Use specific examples of your experience working collaboratively on projects. Discuss your role, the objectives, and how you communicated and coordinated with members of the team to ensure successful project completion.

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How do you stay updated with advancements in biopharmaceutical testing?

Share your strategies for staying informed about advancements in biopharmaceutical testing, such as subscribing to scientific journals, attending industry conferences, and participating in relevant training or webinars.

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Why do you want to work as a Bioassay Analyst at Eurofins?

When answering this question, align your response with Eurofins’ mission of safety and sustainability. Express your enthusiasm for contributing to this mission and your eagerness to grow and learn within the company’s structured support environment.

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How do you ensure accuracy and attention to detail in your work?

Discuss your processes for ensuring accuracy, such as double-checking results, using standardized procedures, and maintaining a thorough documentation process. Emphasize the importance of attention to detail in ensuring compliance and quality in analytical testing.

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What experience do you have with automated liquid handling systems?

Detail your hands-on experience with automated liquid handling systems. Explain how you integrated this technology into your previous work, highlighting efficiencies gained and the complexities managed to ensure reliable assay outcomes.

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In your opinion, what is the most important aspect of method qualification?

Discuss your view on method qualification, underlining the importance of reproducibility, accuracy, and regulatory compliance. Explain how you ensure that all methods meet these standards before they are implemented.

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How would you handle a situation where you received unexpected analytical results?

Share a structured response plan for unexpected analytical results. Focus on investigating the cause, recalibrating equipment if necessary, and how you would communicate with your team to address the anomaly and determine the next steps.

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DATE POSTED
April 9, 2025

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