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Pilot Facility Process Technician

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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

Job Description

  • Prepare both small (less than 200L) and large (200L-500L) volume buffers and tissue culture media for various R&D science lines and pilot manufacturing requested by science line customers, as described in standard operating procedures
  • Set up, execute, and evaluate non-GMP unit operations such as bioreactors, centrifugation, filtration, chromatography, ultrafiltration/diafiltration and final fill
  • Execute Clean-in-Place (CIP), Sterilize-in-Place (SIP), aseptic sampling, parts washing, inventory management, documentation, work order generation, and data entry/evaluation
  • Perform algebraic mathematical calculations and determine molarity, molality, and percentages
  • Calculate volumes of required solution components based on mathematical calculations

Qualifications

The Ideal Candidate will Have Experience with: 

  • Buffer and media preparation (small & large volumes) for R&D and pilot manufacturing
  • Non-GMP unit operations: bioreactors, centrifugation, filtration, chromatography, ultrafiltration/diafiltration, final fill
  • CIP/SIP execution, aseptic sampling, parts washing, inventory management, and documentation
  • Work order generation, data entry, and evaluation
  • Algebraic calculations, including molarity, molality, percentages, and solution component volumes

Minimum Qualifications: 

  • HS Diploma + 2 years of experience in a laboratory or manufacturing environment (bioprocess or chemical process industry) or AS in a scientific field with some related experience
  • Demonstrated capability to work as a team member in a matrix environment
  • Strong mechanical aptitude and demonstrated ability to interface with automated systems
  • Dedication to maintaining and operating in a safe work environment
  • Ability to work independently and adapt to rapidly changing priorities
  • Understanding of continuous improvement tools (LEAN/Six Sigma, 5S, etc)
  • Proficiency in Microsoft Word and Excel

Physical Requirements

  • Work in an indoor laboratory environment where more than 85% of work is accomplished while standing
  • Walk distances between buildings and up and down stairs
  • Bend at the knees and waist for a variety of lifting activities
  • Transport items between floors/buildings weighing up to 500 lbs with the use of assisted moving equipment (lifts, motorized carts, etc.)
  • Move large quantities of raw materials and media powders (up to 90lbs with assisted lifting equipment) and large volume liquid stocks (up to 20L)
  • Handle some hazardous materials requiring the use of personal protective equipment and follow good laboratory practices (GLP) at all times

Additional Information

What to Expect in the Hiring Process: 

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

Additional Details: 

The position is full-time, on-site Mon-Fri 6:30 am-2:30 pm. Overtime will be required on a rotational basis to cover weekend Bioreactor sampling and occasional off-shift operations. Candidates living within a commutable distance of Andover, MA, and the surrounding areas are encouraged to apply. 

Excellent full-time benefits including comprehensive medical coverage, dental, and vision options, also include:

  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays

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

$60000 / YEARLY (est.)
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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 Pilot Facility Process Technician, Eurofins

Join Eurofins Scientific as a Pilot Facility Process Technician in Andover, MA, where you'll become an integral part of a company that champions sustainability and safety in our food, water, and pharmaceuticals. This role is perfect for those with passion and experience in laboratory and manufacturing environments. In this position, you'll prepare both small and large volume buffers and tissue culture media for various R&D science lines and pilot manufacturing, following detailed standard operating procedures. You'll have the opportunity to set up and execute key non-GMP unit operations including bioreactors, centrifugation, and chromatography, ensuring everything runs smoothly and effectively. Attention to detail is paramount, as you'll perform algebraic calculations to determine essential solution components and their respective volumes. Your strong mechanical aptitude will shine as you work collaboratively in a dynamic team, engaging with automated systems to enhance our processes. If you thrive in a setting that values adaptability and continuous improvement, this is the role for you. Eurofins offers excellent benefits and a supportive environment that empowers you to make impactful contributions to science and safety every day. Explore this exciting opportunity where your skills can truly make a difference!

Frequently Asked Questions (FAQs) for Pilot Facility Process Technician Role at Eurofins
What are the main responsibilities of a Pilot Facility Process Technician at Eurofins Scientific?

As a Pilot Facility Process Technician at Eurofins Scientific, your primary responsibilities will include preparing various buffer solutions and media for both small and large volumes, executing non-GMP unit operations like centrifugation and chromatography, and performing essential tasks such as cleaning and maintaining equipment. You'll be involved in critical calculations related to solution preparation, all while adhering to strict safety and quality standards.

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What qualifications do I need to become a Pilot Facility Process Technician at Eurofins Scientific?

To qualify for the Pilot Facility Process Technician position at Eurofins Scientific, candidates should have at least a high school diploma with two years of laboratory or manufacturing experience in bioprocess or chemical processes. Alternatively, an associate degree in a scientific field is acceptable with some related experience. Ideally, you should demonstrate strong mechanical aptitude and teamwork capabilities.

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What is the work environment like for a Pilot Facility Process Technician at Eurofins Scientific?

The work environment for a Pilot Facility Process Technician at Eurofins Scientific is primarily indoor and laboratory-based, where you will be standing for most of the day. Physical activities including lifting and transporting materials are common, and personal protective equipment is required to ensure safety while handling certain materials.

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What additional skills are beneficial for a Pilot Facility Process Technician at Eurofins Scientific?

In addition to your core qualifications, having a solid understanding of continuous improvement tools such as LEAN and Six Sigma can be highly beneficial for a Pilot Facility Process Technician at Eurofins Scientific. Proficiency in Microsoft Office applications, particularly Excel and Word, will also support your performance in documenting and evaluating data effectively.

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What are the job hours for a Pilot Facility Process Technician at Eurofins Scientific?

The position of Pilot Facility Process Technician at Eurofins Scientific has a full-time schedule, typically from Monday to Friday, 6:30 am to 2:30 pm. Overtime may be required on a rotational basis to cover weekend bioreactor sampling and other occasional off-shift operations, providing added flexibility for those who can accommodate it.

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Common Interview Questions for Pilot Facility Process Technician
How do you ensure accuracy when performing buffer and media preparation as a Pilot Facility Process Technician?

To ensure accuracy during buffer and media preparation, it's essential to meticulously follow standard operating procedures, perform manual calculations accurately, and verify measurements multiple times. Additionally, continuous review of your process and adherence to safety protocols can ensure product integrity and safety.

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Can you explain a non-GMP unit operation you've worked with as a Pilot Facility Process Technician?

Certainly! I have experience with bioreactors, where I set up the equipment, monitored conditions, and executed growth phases for various cell types. Understanding the parameters that affect cell growth and product yield is critical, and I relied on diligent data collection to optimize the process.

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What steps do you take to maintain a safe laboratory environment?

Maintaining a safe laboratory environment involves regularly inspecting equipment, adhering to safety protocols, properly using personal protective equipment, and ensuring that all hazardous materials are handled according to good laboratory practices. Participating in safety training sessions and encouraging open communication can also help ensure everyone's safety.

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Describe your experience with Clean-in-Place (CIP) systems.

In my previous roles, I operated CIP systems to clean and sanitize equipment without disassemblage. I carefully followed the prescribed cleaning cycles, monitored chemical concentrations, and verified that all equipment was sanitized properly before production commenced to ensure compliance with safety standards.

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What challenges have you faced while working with chromatography processes?

One challenge I've faced while working with chromatography was troubleshooting inefficiencies in resolution. I addressed this by reviewing flow rates, buffer composition, and column conditions. Additionally, collaborating with colleagues to gather insights and optimize the methods proved invaluable to overcoming the issue.

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How do you manage your time effectively in the lab?

Effective time management in the lab comes from prioritizing tasks, using checklists to track progress, and being adaptable to changing priorities. I break larger projects into manageable steps while maintaining communication with team members to ensure alignment on deadlines and responsibilities.

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What is your approach to teamwork in a matrix environment?

In a matrix environment, I emphasize open communication and trust. I engage with team members to share insights and assist each other in meeting project goals. Additionally, I adapt to different working styles and ensure that everyone's contributions are recognized and valued.

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How do you approach learning new technologies?

When learning new technologies, I take a systematic approach by seeking out training resources, collaborating with experienced colleagues, and hands-on practice. I find that asking questions and actively engaging with the technology helps solidify my understanding and ensure that I remain current in my field.

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How do you handle hazardous materials in the laboratory?

Handling hazardous materials involves a strict adherence to safety protocols, proper usage of personal protective equipment, and thorough training on material safety data sheets. Additionally, I maintain an organized workspace and ensure proper labeling and storage of hazardous substances to minimize risks.

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What can you tell us about your experience with maintaining documentation in the lab?

In my previous roles, I prioritized maintaining accurate and thorough documentation for every process. I ensured that all data entries were completed immediately and double-checked for accuracy. This diligence not only supports compliance during audits but also fosters effective collaboration within the team.

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Full-time, on-site
DATE POSTED
March 26, 2025

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