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Engineer 2, Upstream - MSAT

Position Overview

The Upstream Engineer/Scientist 2 will provide tech transfer support and technical oversight for a large-scale cell culture in monoclonal antibody manufacturing.

Company Overview

Follow Your Genki to North America's largest, state-of-the-art Life Science Manufacturing Facility & CDMO

The work we do at FUJIFILM Diosynth Biotechnologies has never been more important—and we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in people’s lives. Join FUJIFILM Diosynth Biotechnologies and help manufacture the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe. We are proud to cultivate a culture that will fuel your passion, energy and drive - what we call Genki.

 

Join us

We are growing our locations and are investing more than $2 billion into establishing a new large-scale manufacturing site for biopharmaceuticals in the United States to accelerate the growth of our Bio CDMO (Contract and Development Manufacturing Organization) business. This will be the largest end-to-end cell culture CDMO provider in North America.

 

The new site will offer end-to-end solutions to our customers looking to manufacture biopharmaceuticals in the US. In addition to drug substance manufacture, it will also provide automated fill-finish and assembly, packaging, and labeling services. The new state-of-the-art facility is located in Holly Springs, North Carolina, United States.

 

Job Description

What You’ll Do

  • Conducts lab and pilot plant experiments
  • Generates and coordinates execution sampling protocols
  • Serves as subject matter expert (SME) to lead and conduct troubleshooting, process impact assessments, and executes root cause analysis (RCA) and corrective and preventive action (CAPA) in response to deviations
  • Executes and analyzes lab and pilot plant work aimed at solving complex manufacturing problems
  • Leads and supports technology transfer (TT) across multiple unit operation
  • Coordinates, plans, and executes manufacturing process validation runs
  • Supports design and leads generation of sampling plans for process validation reports (PVRs) and investigations
  • Writes and reviews master batch records (MBRs) and standard operating procedures (SOPs), as needed
  • Generates and executes process training and consults on topics related to manufacturing and process
  • Leads technical risk assessments for new manufacturing processes
  • Contributes to the management of manufacturing data (i.e., databasing) and the statistical analysis aimed at both process monitoring and  continued process verification
  • Writes documentation for internal and external use, such as manufacturing campaigns summary reports, process performance qualification (PPQ) protocol and reports, impact assessments etc.
  • Leads training of manufacturing staff and process sciences group on new processes, procedures, and use of equipment in the lab
  • Interprets and utilizes new knowledge to promptly drive data-based decisions
  • Collaborates with the manufacturing department to support commercial and clinical manufacturing campaigns, including on-floor support
  • Leads continuous improvement projects within unit operations, in partnership with manufacturing when applicable, to improve manufacturability,  reliability, yield and cost
  • Supports supplier technical evaluations, risk assessments, and raw material evaluation and qualification
  • Other duties, as assigned

Knowledge and Skills

  • Proficient knowledge in Design of Experience (DOE)
  • Proficient knowledge in Statistical Process Control
  • Effective communication, both written and oral
  • Ability to effective present information to others
  • Proficient project management skills
  • Advanced problem-solving skills
  • Ability to provide feedback to others, including leaders
  • Ability to develop effective working relationships internally and externally
  • Ability to adapt communication style to differing audiences and advise others on difficult matters

Basic Requirements

  • Associate degree in Engineering, Life Science or Chemical Engineering with 4 years of related work experience (e.g., manufacturing); or
  • Bachelor’s degree in Engineering, Life Science or Chemical Engineering with 2 years of related work experience (e.g., manufacturing); or 
  • Master’s degree with no prior experience
  • Experience using quality systems (e.g., deviation management, change control, CAPA, document management system)
  • Experience in contract manufacturing or interacting with contract manufacturers

Preferred Requirements

  • Experience working in a Good Manufacturing Practices (GMP) environment

WORKING CONDITIONS & PHYSICAL REQUIREMENTS

Will work in environment which may necessitate respiratory protection X No YesMay work in Mechanical/Production spaces that may require hearing protection and enrollment in a hearing conservation program. X No Yes Will work in environment operating a motor vehicle or Powered Industrial Truck. X No Yes Ability to discern audible cues. No X YesAbility to inspect or perform a task with 20/20 corrected vision, visual acuity, including distinguishing color. X No Yes

Ability to ascend or descend ladders, scaffolding, ramps, etc. X No YesAbility to stand for prolonged periods of time. X No Yes Ability to sit for prolonged periods of time. X No Yes Ability to conduct activities using repetitive motions that include writs, hands and/or fingers. X No YesAbility to operate machinery and/or power tools. X No YesAbility to conduct work that includes moving objects up to X pounds. X No Yes If yes, 10 lbs. 33 lbs.Ability to bend, push or pull, reach to retrieve materials from 18” to 60” in height, and use twisting motions. X No Yes

 

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.

EEO Information

Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.

ADA Information

If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBN_PNC@fujifilm.com).

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CEO of FUJIFILM
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Teiichi Goto
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Average salary estimate

$75000 / YEARLY (est.)
min
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$60000K
$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 Engineer 2, Upstream - MSAT, FUJIFILM

Are you an aspiring engineering professional with a passion for biopharmaceutical manufacturing? Look no further than the Engineer 2, Upstream position at FUJIFILM Diosynth Biotechnologies, based in the vibrant city of Holly Springs. In this pivotal role, you'll be at the helm of technological advancement, supporting tech transfer and ensuring seamless operations in our cutting-edge monoclonal antibody manufacturing process. Your responsibilities will range from conducting lab experiments to leading troubleshooting efforts and executing root cause analysis to secure the highest quality standards in production. With FUJIFILM Diosynth at the forefront of biopharma innovation, your work will directly contribute to the manufacturing of life-changing therapies and vaccines, partnering with some of the most dynamic biotech companies worldwide. Collaborate with a talented team as you coordinate process validation runs and develop effective training initiatives, all while championing continuous improvement projects that enhance manufacturability and efficiency. This is your chance to challenge yourself and grow within a company that embraces the spirit of 'Genki'—positive energy and unwavering motivation—while investing over $2 billion to expand our capabilities. If you hold an engineering or life sciences degree and have some experience in a manufacturing setting, this role could be your stepping stone to making a real difference in people's lives through science. Join us at FUJIFILM Diosynth Biotechnologies and embark on a rewarding career where the power of technology meets the mission of helping others.

Frequently Asked Questions (FAQs) for Engineer 2, Upstream - MSAT Role at FUJIFILM
What are the responsibilities of the Engineer 2, Upstream at FUJIFILM Diosynth Biotechnologies?

The Engineer 2, Upstream at FUJIFILM Diosynth Biotechnologies plays a crucial role in supporting tech transfer processes, conducting lab experiments, and ensuring smooth operations in monoclonal antibody manufacturing. This includes troubleshooting, process assessments, leading technology transfer across various operations, and managing process validation runs effectively.

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What qualifications are required for the Engineer 2, Upstream position at FUJIFILM Diosynth Biotechnologies?

Candidates should possess at least an Associate's degree in Engineering, Life Science, or Chemical Engineering with relevant experience in manufacturing, or a Bachelor's degree with less experience. A Master’s degree is also acceptable with no prior experience. Familiarity with quality systems and Good Manufacturing Practices (GMP) is advantageous.

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How does the Engineer 2, Upstream role contribute to manufacturing biopharmaceuticals at FUJIFILM Diosynth Biotechnologies?

The Engineer 2, Upstream significantly contributes by ensuring the successful execution of lab experiments and validating manufacturing processes that are pivotal in delivering high-quality biopharmaceuticals. Their tasks also involve supporting the training of staff and driving continuous improvement to meet and exceed manufacturing standards.

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What skills are beneficial for the Engineer 2, Upstream role at FUJIFILM Diosynth Biotechnologies?

Essential skills for the Engineer 2, Upstream role include advanced problem-solving, effective communication, project management expertise, and proficiency in statistical process control. An understanding of Design of Experiment (DOE) and the ability to collaborate on complex manufacturing challenges are also key.

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What is the work environment like for the Engineer 2, Upstream at FUJIFILM Diosynth Biotechnologies?

The work environment for the Engineer 2, Upstream at FUJIFILM Diosynth Biotechnologies involves both lab settings and manufacturing spaces that may require specific safety measures such as respiratory protection. Employees will often be involved in physically demanding tasks, which could include prolonged standing and working with heavy materials.

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Common Interview Questions for Engineer 2, Upstream - MSAT
Can you describe your experience with laboratory experiments relevant to the Engineer 2, Upstream role?

When answering this question, highlight specific laboratory techniques you've employed, particularly in the context of biopharmaceutical manufacturing. Discuss your familiarity with experiments related to monoclonal antibodies and any relevant outcomes that can demonstrate your contributions to process improvements.

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How do you approach troubleshooting complex manufacturing processes?

In your response, emphasize a structured approach to troubleshooting that includes gathering data, conducting root cause analysis, and implementing corrective actions. Providing a real-world example where you successfully troubleshot a complex issue will strengthen your answer.

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What is your understanding of Good Manufacturing Practices (GMP) and why are they important?

Your answer should encompass a brief overview of GMP principles and the importance of maintaining product quality and safety in biopharmaceutical manufacturing. Share any direct experiences you have working under GMP guidelines to illustrate your understanding.

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Discuss a continuous improvement project you've been involved with in your previous roles.

When addressing this question, share details about the project, what prompted the initiative, your role in implementing it, and the measurable outcomes. This shows your initiative and capability to enhance manufacturing processes.

Join Rise to see the full answer
How do you ensure effective communication when leading a team or project?

Discuss your strategies for facilitating communication among team members, such as regular check-ins, feedback sessions, and adapting your communication style to fit the audience. Highlight experiences where strong communication led to project success.

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What analytical tools do you use for process monitoring and improvement?

Here, mention tools you are familiar with, such as statistical process control charts, design of experiments software, or other analytics platforms. Elaborate on how you've applied these tools to improve manufacturing efficiency or product quality.

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How do you handle tight deadlines in a manufacturing environment?

Share your approach to prioritizing tasks, managing time effectively under pressure, and maintaining quality standards while meeting deadlines. Providing an anecdote where you successfully met a challenging deadline could strengthen your response.

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Explain how you would train staff on new processes or equipment.

Discuss your training methodology, including how you assess team members’ understanding, the importance of shadowing or hands-on experience, and using visual aids or documentation. Highlight any past experiences where you effectively trained others.

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What safety measures do you implement while conducting experiments?

When answering, emphasize your commitment to safety by mentioning protocols you follow, including proper use of protective equipment and adherence to safety guidelines. Illustrating an incident where safety procedures were critical can add depth to your response.

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Why do you want to work as an Engineer 2, Upstream at FUJIFILM Diosynth Biotechnologies?

Express your passion for biopharmaceutical manufacturing and how FUJIFILM's mission aligns with your career aspirations. Share specific aspects of the company or role that excite you, emphasizing how you see yourself contributing to their goals.

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Full-time, on-site
DATE POSTED
April 16, 2025

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