QC Microbiology Supervisor — Lead in cGMP Lab (Wed–Sat)

FUJIFILM Electronic Materials (Europe) N.V.; North Carolina; On-site; USD 95,000 - 130,000; Full time

Benefits offered by this job

On-site perks

Job summary

FUJIFILM Biotechnologies in North Carolina seeks a Supervisor, QC Microbiology to lead a team of analysts ensuring GMP testing and environmental monitoring. The role focuses on data integrity, right first time performance, and continuous improvement.

You will supervise 6–12 analysts, manage training, CAPAs, and participate in cross-functional initiatives. This onsite role requires a Bachelor's in Life Science and cGMP experience.

Qualifications

• Bachelor's degree in Life Science with 4+ years in a cGMP environment.
• Experience leading QC Micro analysts and managing training.
• Familiarity with cGMP, data integrity, and regulatory expectations.
• Knowledge of LIMS/ELN and eQMS systems.
• Experience with CAPA, investigations, and change controls.
• Comfortable with audits and inspection readiness.
• Knowledge of environmental monitoring and aseptic techniques.

Responsibilities

• Lead QC Micro analysts; supervise scheduling, training, and performance.
• Oversee environmental monitoring and utilities programs.
• Review data, test records, COAs; ensure ALCOA+ data integrity.
• Manage sample logistics, inventory, and equipment readiness.
• Lead or approve deviations, OOS/OOT investigations, CAPAs.
• Contribute to risk assessments, trend reports, and quality systems.
• Support audits and regulatory inspections.

Skills

People leadership

cGMP compliance

Data integrity

LIMS/ELN familiarity

SOPs/Validation

Lean/Six Sigma

Cross functional collaboration

Education

Bachelor's in Life Science

Tools

LIMS/ELN

TrackWise

MS Office

Job description

FUJIFILM Biotechnologies in North Carolina seeks a Supervisor, QC Microbiology to lead a team of analysts ensuring GMP testing and environmental monitoring. The role focuses on data integrity, right first time performance, and continuous improvement.

You will supervise 6–12 analysts, manage training, CAPAs, and participate in cross-functional initiatives. This onsite role requires a Bachelor's in Life Science and cGMP experience.