Scientist 1, QC Chemistry

FUJIFILM; Holly Springs (AL); On-site; USD 95,000 - 125,000; Full time

Job summary

FUJIFILM Biotechnologies in Holly Springs, NC, seeks a Scientist 1, QC Chemistry to perform QC analytical testing on biological products, including chromatography (GC, HPLC, UPLC, SEC), spectroscopy (MS, LC-MS/MS, UV), icIEF, glycan analysis, and particle analysis. Ensure GMP-compliant operations and approve results.

You will develop and review SOPs, support tech transfer and routine manufacturing, provide training, and collaborate across QC, Manufacturing, Process Science, and QA.

Qualifications

• Bachelor’s in Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field with 5+ years of experience; OR Master’s with 3+ years; OR PhD with 1+ year.
• GMP-regulated laboratory experience in biotechnology, pharma, CRO or CLO.
• Experience with physical/chemical analytical methods (GC, HPLC, UPLC, SEC; MS; UV/Vis; FTIR; icIEF; etc.).

Responsibilities

• Perform physical and chemical analytical testing for biological products per GMP.
• Ensure testing of DS/DP/stability samples per GMP regulations.
• Peer review analytical data and support tech transfer and manufacturing.
• Validate methods and maintain laboratory equipment.
• Draft and review SOPs, CAPAs, deviations, and change controls.
• Collaborate across QC, Manufacturing, Process Science and QA.

Skills

English communication

Oral and written communication

Project leadership

Data analysis

Cross-functional collaboration

Attention to detail

Independent work

Education

Bachelor’s in Chemistry or related field

Master’s in Chemistry or related field

PhD in Chemistry or related field

Tools

LIMS

TrackWise

Job description

Position Overview

The Scientist 1, QC Chemistry is responsible for QC analytical chemistry methods used in biological product manufacturing, including chromatography (GC, HPLC, UPLC, SEC), spectroscopy (MS, GC/MS, LC-MS/MS, UV, UV-Vis, FTIR), electrophoresis (GE, non-reducing and reducing CE-SDS, imaged capillary isoelectric focusing (icIEF)), wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance, etc. The Scientist 1, QC Chemistry ensures GMP-compliant laboratory operations in accordance with regulatory guidelines. This role performs technical/compliance reviews and approves analytical results. The role approves laboratory exceptions, invalid assays, deviations, change controls, and corrective and preventative actions (CAPAs).

Company Overview

FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we’ll open North America’s largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.

We’re looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we’re proud to cultivate a culture that will fuel your purpose, energy, and drive—what we call Genki. Ready to shape the future of medicine? Let’s transform healthcare together!

Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh’s thriving tech scene, making it the perfect blend of community and opportunity.

Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: https://www.fujifilm.com/us/en/about/region/careers

Job Description

What You’ll Do

• Performs physical and chemical analytical testing methods for biological products, including chromatography (GC, HPLC, UPLC, SEC), spectroscopy (MS, GC/MS, LC-MS/MS, UV, UV-Vis, FTIR), electrophoresis (GE, non-reducing and reducing CE-SDS, imaged capillary isoelectric focusing (icIEF)), wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance.
• Ensures analytical testing of in-process, drug substance (DS), drug product (DP), and stability samples is performed according to appropriate GMP regulations.
• Performs laboratory work and peer reviews of analytical data in support of tech transfer and routine manufacturing.
• Executes and reviews method qualification and validation activities and maintains lab equipment.
• Monitors assay performance and implements improvements that ensure quality and efficiency within QC Chemistry.
• Troubleshoots and investigates deviations and invalid assays performed in QC Chemistry.
• Authors, reviews, and approves SOPs, protocols, reports, change controls, Trackwise deviations, out-of-specification (OOS) and out-of-trend (OOT) investigations, and CAPAs for the QC Chemistry team, as needed.
• Participates in cross-functional collaborations with other QC Departments, Manufacturing, Process Science, and Quality Assurance stakeholders to achieve customer and FUJIFILM Biotechnologies objectives.
• Manages and monitors lab activities, as needed.
• Provides training for QC Chemistry associates.
• Provides technical support as the QC Chemistry SME during customer visits, audits, and regulatory inspections.
• Participates in risk and gap assessments during project scoping, as needed.
• Collaborates with the LIMS team and IT department to build new method functionality that meets end‑user and customer requirements.
• Liaises with Contract Laboratory Organizations (CLOs) to monitor method execution and the timely delivery of results, as needed.
• Executes routine analytical methods and trains other QC Chemistry laboratory associates.
• Performs other duties, as assigned.

Knowledge, Skills or Abilities

• Excellent oral and written communications skills and fluency in English; Good computer skills.
• Excellent organization skills and attention to detail.
• Ability to lead improvement projects.
• Self-driven, dedicated, systematic, and able to plan projects and deliverables in a structured way.
• Ability to analyze and present data and technical information to others outside of the team.
• Ability to deliver independently, as well as provide guidance to QC team members. Initiator, motivator, mentor for other team members.
• Ability to develop and assign tasks. Ability to develop structured plans.
• Ability to solve complex challenges and assist others as needed.
• Thinks strategically, ability to plan and implement improvements.
• Passion for customers, ability to act as POC for clients in the laboratory.
• Flexible, with a positive attitude, positive energy and seeks challenges and opportunities.
• Ability to work cross-functionally with a diverse team and represent the department.
• Must be flexible to support 24/7 manufacturing facility.

Minimum Qualifications

• Bachelor’s in Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field with 5+ years of experience; OR,
• Master’s in Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field with 3+ years of experience; OR,
• D. in Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field with 1+ years of experience.
• Analytical laboratory experience preferably in biotechnology, Pharma, Contract Research Organization (CRO), or Contract Laboratory Organization (CLO).
• 3+ years of experience working in a regulated GMP environment.
• Knowledge and experience of physical and chemical analytical testing methods for biological products, including chromatography (GC, HPLC, UPLC, SEC), spectroscopy (MS, GC/MS, LC-MS/MS, UV, UV-Vis, FTIR), electrophoresis (GE, non-reducing and reducing CE-SDS, imaged capillary isoelectric focusing (icIEF)), wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance.

Preferred Qualifications

• 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 preventative action (CAPA), document management system).

Physical Requirements:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. While performing the duties of this job, the employee is required on a regular basis to:

• Ability to discern audible cues.
• Ability to inspect or perform a task with 20/20 corrected vision, visual acuity, including distinguishing color.
• Ability to ascend or descend ladders, scaffolding, ramps, etc…
• Ability to stand for prolonged periods of time up to 60 minutes.
• Ability to sit for prolonged periods of time up to 60 minutes.
• Ability to conduct activities using repetitive motions that include wrist, hands and/or fingers.
• Ability to conduct work that includes moving objects up to 10 pounds.
• Ability to bend, push or pull, reach to retrieve materials from 18’’ to 60’’ in height, and use twisting motions.
• Will work in smal and/or enclosed spaces.
• Will work in heights greater than 4 feet.

*LI-Onsite

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 ([e-mail]).