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Upstream Vaccines Process Development Engineer

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

Employee Responsibilities:

  • Supporting the team in the set-up, operation, and associated analysis of mammalian cell culture and bioreactor processes at a pilot scale
  • General operations such as bioreactor building/sterilization, cleanup and turnover of bioreactors to maintain a set run schedule
  • Sampling including cell count and metabolite analysis
  • Prepare solutions and culture media
  • Perform data analysis
  • Maintain records and test results following good manufacturing practices (GMP)
  • Management of lab supplies and raw materials
  • Work independently and efficiently
  • Document work clearly and perform tests accurately
  • Communicate effectively with client staff members

Qualifications

Minimum Qualifications:

  • Bachelor's degree in in Chemical Engineering, Biomedical Engineering, or Biological Sciences, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)
  • Ability to work weekends and overnight hours as needed
  • Authorization to work in the United States indefinitely without restriction or sponsorship

The Ideal Candidate would possess:

  •  At least six months related laboratory experience including aseptic and cell culture techniques either in a lab scale or pilot scale setting
  • General laboratory skills, including experience with pipettes
  • Experience using formulas and linking spreadsheets in Excel
  • 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

Additional Information

This position is Full-Time, Monday - Friday, 8:00 a.m. - 5:00 p.m. with overtime as needed and the potential for some off shift hours as dependent on project. Candidates currently living within a commutable distance of West Point, PA 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

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

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Average salary estimate

$80000 / YEARLY (est.)
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$70000K
$90000K

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 Upstream Vaccines Process Development Engineer, Eurofins

Are you ready to take your career to the next level as an Upstream Vaccines Process Development Engineer at Eurofins Scientific? Located in West Point, PA, Eurofins is not just another life sciences company; it's a leader in providing a vast range of analytical testing services that help ensure our environment and health are prioritized. In this role, you'll dive into the exciting world of bioreactor processes and mammalian cell culture, supporting the team in everything from set-up to data analysis. Your hands-on work will involve the entire lifecycle of bioreactors—building, sterilization, and maintenance—to maintain our schedule while adhering to good manufacturing practices (GMP). You’ll also be responsible for critical tasks like sampling cell counts, preparing media solutions, and managing laboratory supplies. Maintaining clear documentation and communicating effectively will be key, ensuring our projects run smoothly. We're looking for someone with a Bachelor's degree in Chemical Engineering, Biomedical Engineering, or Biological Sciences, and at least six months of relevant lab experience. If you thrive in a team environment, possess strong organizational skills, and have an eagerness to learn, then this is the perfect opportunity for you. Join us and contribute to making life and our environment safer, healthier, and more sustainable at Eurofins Scientific!

Frequently Asked Questions (FAQs) for Upstream Vaccines Process Development Engineer Role at Eurofins
What are the responsibilities of an Upstream Vaccines Process Development Engineer at Eurofins Scientific?

At Eurofins Scientific, an Upstream Vaccines Process Development Engineer is responsible for supporting the set-up, operation, and analysis of mammalian cell culture and bioreactor processes at a pilot scale. This role involves bioreactor construction, sterilization, sampling, data analysis, and maintaining accurate records in compliance with good manufacturing practices (GMP).

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What qualifications are required for the Upstream Vaccines Process Development Engineer position at Eurofins Scientific?

To qualify for the Upstream Vaccines Process Development Engineer role at Eurofins Scientific, candidates must have a Bachelor's degree in Chemical Engineering, Biomedical Engineering, Biological Sciences, or a related field. Additionally, six months of laboratory experience and the ability to work independently as well as as part of a team are essential.

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What skills are important for an Upstream Vaccines Process Development Engineer at Eurofins Scientific?

Key skills for an Upstream Vaccines Process Development Engineer at Eurofins Scientific include strong scientific and computer skills, excellent communication abilities, meticulous attention to detail, and the ability to learn new techniques. Experience with aseptic and cell culture techniques is also beneficial.

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What is the work schedule like for the Upstream Vaccines Process Development Engineer at Eurofins Scientific?

The Upstream Vaccines Process Development Engineer position at Eurofins Scientific is full-time, typically from Monday to Friday, 8:00 a.m. to 5:00 p.m. However, there's potential for some overtime and off-shift hours depending on project needs.

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What benefits do Upstream Vaccines Process Development Engineers receive at Eurofins Scientific?

Eurofins Scientific offers excellent benefits for Upstream Vaccines Process Development Engineers, including comprehensive medical coverage, dental and vision options, life and disability insurance, a 401(k) with company match, and paid vacation and holidays.

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Common Interview Questions for Upstream Vaccines Process Development Engineer
Can you describe your experience with mammalian cell culture techniques?

When answering this question, provide specific examples of your experience with mammalian cell cultures, emphasizing any protocols you've followed or challenges you've overcome. Discuss how these experiences have prepared you for the Upstream Vaccines Process Development Engineer role.

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How do you ensure compliance with good manufacturing practices (GMP) in a lab setting?

Address your understanding of GMP and share your past experiences related to compliance. Highlight specific practices you implemented to maintain GMP standards in laboratory work as an Upstream Vaccines Process Development Engineer.

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Describe a situation where you had to troubleshoot a bioreactor process.

Provide a detailed account of a bioreactor-related issue you faced, the steps you took to diagnose the problem, and the resulting solution. This will showcase your analytical skills and ability to work under pressure.

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What data analysis software are you familiar with, and how do you use it?

Discuss any data analysis tools you've used, such as Excel or specialized software. Explain how you've utilized these tools to analyze bioprocess data, drawing connections to the Upstream Vaccines Process Development Engineer responsibilities.

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How do you prioritize your tasks when working on multiple projects?

Explain your approach to time management and project prioritization. Share strategies that have worked for you in the past, emphasizing your ability to adapt in a fast-paced environment.

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What strategies do you use for effective communication with team members and clients?

Emphasize your communication skills and provide examples of how you have effectively shared information with colleagues or clients. Highlight your ability to adapt your communication style based on the audience.

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Can you discuss your experience with bioreactor operations?

Talk about the specific roles you have played in bioreactor operations, the types of bioreactors you've worked with, and any related processes you've implemented. Relate this to the requirements of the Upstream Vaccines Process Development Engineer position.

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How do you keep accurate records in the lab, and why is it important?

Discuss your record-keeping practices, emphasizing their importance for compliance and project success. Provide examples of how proper documentation has benefited your previous projects.

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What motivates you to work in the field of vaccines and bioprocess development?

Share your passion for the life sciences field and how it aligns with your career goals. Explain how the mission of Eurofins Scientific resonates with your desire to make an impact in public health.

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What ongoing learning opportunities do you seek in your career?

Talk about your commitment to continuous improvement and professional development. Mention any training or courses you're interested in that would enhance your skills as an Upstream Vaccines Process Development Engineer.

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Full-time, on-site
DATE POSTED
March 27, 2025

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