Enter a job title or keyword

Senior Analyst 1, QC Analytical Development Chemistry

Job Location:

Holly Springs, MS - USA

Monthly Salary: Not provided by the employer

Posted: 2 October 2026 (14 hours ago)

Application Deadline: 30 December 2026

Vacancies: 1 Vacancy

Register to Apply

Job Summary

Position Overview

The Senior Analyst 1 QC Analytical Development (AD) Chemistry works with limited direction to support the execution of analytical method transfers and validations for drug substance (DS) and drug product (DP) manufacturing into the Quality Control laboratories of FUJIFILM Biotechnologies Holly Springs. The analytical chemistry methods used in biological product manufacturing include chromatography spectroscopy electrophoresis wet chemistry glycan analysis sub-visible particle analysis peptide mapping and physical appearance etc. The Senior Analyst 1 QC AD Chemistry adheres to GMP compliant laboratory operations in accordance with regulatory guidelines. This role executes analytical method transfers from clients and authors and reviews procedures SOPs and technical reports.

Company Overview

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

Were 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 were proud to cultivate a culture that will fuel your purpose energy and drivewhat we call Genki. Ready to shape the future of medicine Lets transform healthcare together!

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

Fujifilm is globally headquartered in Tokyo with over 70000 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: Description

What Youll Do

Executes verification transfer and validation of analytical chemistry methods 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. with cellular and molecular analytical testing methods.
Ensures compliance of analytical testing with appropriate GMP regulations.
Participates in regular meetings for TT programs with cross-functional teams and key stakeholders.
Authors and reviews SOPs protocols and technical reports.
Works cross-functionally with Contract Laboratory Organizations (CLOs) QC testing teams Quality Assurance (QA) and Process Science groups to ensure transfer of non-compendial and compendial methods 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.
Supports the QC AD team to investigate any project challenges with necessary risk assessment tools and techniques as needed.
Supports best practices for TT and PPQ strategies globally as required.
Coordinates and supports QC AD Chemistry lab activities as needed.
Provides training for QC Chemistry lab associates.
Utilizes MSDS sheets to properly assess chemical hazards spill response procedures and PPE requirements if indicated.
Performs other duties as assigned.

Knowledge Skills and Abilities

Knowledge of cGMPs ICH USP EP JP and FDA requirements as it relates to physical and chemical analytical methods.
Working knowledge and experience in Microsoft Office products (Outlook Word Excel and Power Point).
Ability to work with minimal supervision.
Ability to effectively communicate and function in a fast-paced highly technical environment is essential to success.
Demonstrated ability to work cross-functionally and to develop and maintain strong business partner relationships.
Excellent verbal and written communication skills and attention to detail.
Thorough understanding of pharmaceutical/biotech testing.
Proven ability to conduct investigations writing deviations and CAPAs.
Superior technical writing and problem-solving skills required.
Must be flexible to support 24/7 manufacturing facility.

Minimum Qualifications

A./B.S. degree in Chemistry Biology Microbiology Biochemistry or other relevant scientific discipline with 2 years of experience; OR
Masters degree in biology Chemistry Biochemistry Microbiology or other relevant scientific discipline with 0 years experience.
3 years laboratory experience.
1-3 years GMP laboratory experience.
Experience in a GMP environment.
Experience with physical and chemical analytical testing 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. with cellular and molecular analytical testing methods.

Preferred Qualifications

Masters degree in Biology Chemistry Biochemistry Microbiology or other relevant scientific discipline with 1 years experience.
Experience with LIMS software.

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 stand for prolonged periods of time for up to 240 minutes.
Ability to sit for prolonged periods of time for up to 240 minutes.
Ability to conduct activities using repetitive motions that include wrists 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 warm/cold environments (5C Range).
Will work in small and/or enclosed spaces.

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 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 committedto 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 ().

Required Experience:

Senior IC

Apply Now

About Company

Fujifilm

View Profile View Profile

AI AutoApply

Apply to 100+ jobs with one click

AI AutoApply

AI Resume Builder

Create an ATS-ready CV in minutes

AI Resume Builder

AI Cover Letter

Write a personalized letter instantly

AI Cover Letter