First-Shift QC Chemistry Supervisor

FUJIFILM Holdings America Corporation; Holly Springs (NC); On-site; USD 110,000 - 140,000; Full time

Job summary

FUJIFILM Biotechnologies in North Carolina seeks a Supervisor, QC Chemistry (First shift) to lead the testing of analytical methods used in biopharmaceutical manufacturing. You will supervise a team performing chromatography, spectroscopy, electrophoresis, glycan analysis, peptide mapping, and physical appearance assessments under cGMP.

The role drives audit readiness, CAPA investigations, and collaboration across QC, Manufacturing, and QA to ensure timely results and continuous improvement.

Qualifications

• Bachelor’s degree in a chemistry-related field with 5+ years of experience, or Master’s with 3+ years.
• 2+ years of team management experience.
• 3+ years in a regulated GMP environment.
• Experience with analytical testing methods (HPLC/UPLC/SEC, GC, UV/Vis, icIEF).
• Knowledge of SOPs, change controls, CAPAs, and deviation management.

Responsibilities

• Supervise QC Chemistry team and manage scheduling.
• Ensure GMP-compliant testing of DS/DP, in-process, and stability samples.
• Lead method validation and troubleshooting for analytical tests.
• Review SOPs, test records, change controls, and investigations.
• Coordinate with CLOs and internal departments to meet timelines.
• Support resource planning and budget activities.
• Provide training and mentorship to team members.

Skills

Team leadership

GMP compliance

Analytical testing

Oral & written communication

Cross-functional collaboration

Audits & inspections

Education

Bachelor’s or Master’s in Chemistry/Biochemistry/Biological Sciences

Tools

LIMS

TrackWise

Smartsheet

Kneat validation

Job description

FUJIFILM Biotechnologies in North Carolina seeks a Supervisor, QC Chemistry (First shift) to lead the testing of analytical methods used in biopharmaceutical manufacturing. You will supervise a team performing chromatography, spectroscopy, electrophoresis, glycan analysis, peptide mapping, and physical appearance assessments under cGMP.

The role drives audit readiness, CAPA investigations, and collaboration across QC, Manufacturing, and QA to ensure timely results and continuous improvement.