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Scientist I, Analytical Development Bioassay

Position Overview

The QC Analytical Development (AD) Bioassay Scientist 1 coordinates the transfer of cell- and plate-based analytical methods for Technology Transfer (TT) of drug substance (DS) and drug product (DP) into the Quality Control laboratories of FUJIFILM Biotechnologies Diosynth Holly Springs (FDBN). The QC AD Bioassay Scientist 1 ensures GMP compliant laboratory operations in accordance with regulatory guidelines. This role periodically interfaces with customers and cross-functional teams to scope bioassay analytical testing plans and achieve project milestones. This role authors/reviews transfer plans, method transfer documents, and transfer summary reports to support tech transfers for QC Analytical Development.

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

 

• Manages analytical method transfer and validation activities for cell- and plate-based Bioassays for the QC Analytical Development team• Supports change controls, out-of-specification (OOS) and out-of-trend (OOT) investigations, and CAPAs for the QC Bioassay team, as needed• Interfaces with customers and program management to identify bioassay analytical needs and perform risk and gap assessments during project scoping• Participates in regular meetings for TT programs with cross-functional teams and key stakeholders• Serves as the QC Analytical Development Bioassay subject matter expert (SME) to author and review SOPs, transfer plans, protocols, and reports as part of the tech transfer process to onboard client programs• Liaises with Contract Laboratory Organizations (CLOs), QC testing teams, Quality Assurance (QA), and Process Science groups to ensure prioritization of non-compendial and compendial method transfer activities according to deadlines• Collaborates with the LIMS team and IT department to build new analytical method functionality that meets end-user and customer requirements• Ensures compendial method oversight and scientific guidelines (e.g. ICH, EMA, FDA, etc.)• Supports regulatory requests and inspections• Performs other duties, as assigned

 

Minimum Requirements:

 

• B.S. in Microbiology, Virology, Biology, Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field with 6+ years of analytical laboratory experience preferably in biotechnology, Pharma, Contract Research Organization (CRO), or Contract Laboratory Organization (CLO)• 1-3 years experience in a GMP environment

 

Preferred Requirements:

 

• M.S. in Virology, Microbiology, Biology, Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field with 4+ years of experience, OR• Ph.D. in Virology, Microbiology, Biology, Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field with 2+ years of experience• Experience with Customer Relationship Management• Prior drug substance or manufacturing experience, including process validation, transfer, commercialization, and manufacturing support and troubleshooting• Experience using quality systems (e.g., deviation management system, change control, corrective and preventive action (CAPA), document management system)

 

Physical and Work Environment Requirements:

 

Ability to inspect or perform a task with 20/20 corrected vision, visual acuity, including distinguishing color.

Ability to stand for prolonged periods of time up to 240 minutes

Ability to sit for prolonged periods of time up to 240 minutes

Ability to conduct activities using repetitive motions that include writs, hands and/or fingers.

Ability to conduct work that includes moving objects up to 10 pounds.

 

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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What You Should Know About Scientist I, Analytical Development Bioassay, FUJIFILM

Join FUJIFILM Diosynth Biotechnologies as a Scientist I in our Analytical Development Bioassay team based in Holly Springs! In this exciting role, you’ll be the go-to person coordinating the transfer of vital analytical methods essential for bringing new drug substances and products to life. You'll work in a state-of-the-art facility that’s at the forefront of life science manufacturing. Your day-to-day responsibilities will involve ensuring compliance in all laboratory operations according to GMP regulations, which is critical for achieving superior quality standards. You will be actively interfacing with customers and cross-functional teams, making sure to understand their needs and drafting bioassay analytical testing plans that contribute towards hitting key project milestones. Additionally, you’ll author and review transfer plans, method transfer documents, and summary reports to support the technology transfer process—keeping everything flowing smoothly. It’s a role where your analytical prowess can shine, and your contributions can make a real difference in developing vaccines, cures, and gene therapies. Beyond technical skills, we’re looking for driven individuals who align with our values of passion and teamwork. If you’re ready to dive into the heart of biopharmaceutical development and partner with some of the world's most innovative companies, we can’t wait to see how you can contribute to our mission. Let’s craft the future of healthcare together!

Frequently Asked Questions (FAQs) for Scientist I, Analytical Development Bioassay Role at FUJIFILM
What are the responsibilities of the Scientist I in Analytical Development Bioassay at FUJIFILM Diosynth Biotechnologies?

As a Scientist I in Analytical Development Bioassay at FUJIFILM Diosynth Biotechnologies, your primary responsibilities include coordinating the transfer of analytical methods for drug substances and products, ensuring that all laboratory operations meet GMP compliance. You'll be preparing and reviewing transfer plans and method transfer documents that support tech transfers, as well as performing risk and gap assessments in collaboration with cross-functional teams. Your proactive engagement with customers to ascertain their bioassay needs will also be a key component of your role.

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What qualifications are needed for the Scientist I position at FUJIFILM Diosynth Biotechnologies?

For the Scientist I position in Analytical Development Bioassay at FUJIFILM Diosynth Biotechnologies, you'll need a Bachelor’s degree in a relevant science field along with at least 6 years of analytical laboratory experience, ideally in a biotechnology or pharmaceutical environment. A Master's degree or Ph.D. in a related field can further enhance your qualifications. Familiarity with quality systems and experience in GMP environments is highly preferred.

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How does the Scientist I position at FUJIFILM Diosynth Biotechnologies contribute to quality control?

As a Scientist I in Analytical Development Bioassay, you play a crucial role in maintaining quality control at FUJIFILM Diosynth Biotechnologies by managing analytical method transfers and validations for various bioassays. Your work ensures that all methods comply with regulatory standards, and you'll actively support the investigations of out-of-specification results, ensuring that every aspect of quality assurance is addressed promptly and effectively.

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What kind of work environment can one expect as a Scientist I at FUJIFILM Diosynth Biotechnologies?

The work environment for a Scientist I at FUJIFILM Diosynth Biotechnologies is dynamic and collaborative, centered around innovation and compliance with scientific guidelines. Located in a state-of-the-art facility, you will work alongside skilled professionals from various disciplines and have access to cutting-edge technologies. The culture promotes teamwork, continuous learning, and a commitment to making a difference in the biopharmaceutical field.

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What are the growth opportunities for a Scientist I at FUJIFILM Diosynth Biotechnologies?

FUJIFILM Diosynth Biotechnologies offers robust growth opportunities for a Scientist I in Analytical Development Bioassay. With significant investments in expanding manufacturing capabilities, there are ample chances for career advancement and skill development. You'll have the opportunity to work on groundbreaking projects, gain expertise in diverse analytical methodologies, and collaborate with top-tier professionals in the industry, all contributing to your professional evolution.

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Common Interview Questions for Scientist I, Analytical Development Bioassay
Can you describe your experience with analytical method development?

When answering this question, discuss specific projects you've worked on, the methods you developed or validated, and the outcomes. Be sure to mention any relevant techniques that align with the work at FUJIFILM Diosynth Biotechnologies.

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How do you ensure compliance with GMP regulations in your work?

Highlight your understanding of regulatory guidelines and specific practices you implement to maintain compliance. Discuss how you document your work, manage deviations, and contribute to audits or inspections.

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What strategies do you use for effective project management in analytical development?

Describe your approach to project timelines, resource allocation, and risk assessment. Mention any project management tools or frameworks you've used successfully, and tie it back to how it impacts quality and timeliness.

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Can you give an example of a successful technology transfer you've been involved in?

Provide details about your role in the technology transfer process, including any challenges faced and how you overcame them. Emphasize collaboration with cross-functional teams and adherence to protocols.

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How do you handle out-of-specification (OOS) results in a laboratory setting?

Discuss your systematic approach to investigating OOS results, including documentation, root cause analysis, and corrective actions taken. This shows your analytical problem-solving skills and how you maintain product integrity.

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What experience do you have collaborating with cross-functional teams?

Share examples of projects where you worked closely with other departments, highlighting communication strategies and how such collaboration enhanced the project outcome.

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What techniques do you find most effective for method validation?

Explain specific validation protocols you've executed, the statistical methods used for ensuring robustness, and any relevant regulatory guidelines like ICH or FDA that you've adhered to throughout the validation process.

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How do you stay current with advancements in analytical techniques?

Discuss resources such as professional journals, workshops, conferences, and networking with peers that help you remain informed about developments in analytical methodologies relevant to your role.

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Describe a time when you had to mentor or train a junior team member.

Offer details on how you approached mentoring, the topics or skills you helped them develop, and the impact of this experience on both the mentee and your personal growth.

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Why are you interested in working at FUJIFILM Diosynth Biotechnologies?

Articulate what specifically attracts you to FUJIFILM Diosynth Biotechnologies, such as its commitment to innovative biopharmaceutical solutions, investment in cutting-edge technology, or the company culture that aligns with your career goals.

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