First-Shift QC Chemistry Supervisor

FUJIFILM Biotechnologies

Holly Springs (NC)

On-site

USD 90,000 - 120,000

Full time

14 days+

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Job summary

FUJIFILM Biotechnologies seeks a Supervisor, QC Chemistry (First Shift) to lead day-to-day operations in the Chemistry laboratory. You will supervise a team performing routine analytical testing for in-process, DS, DP, and stability samples, ensuring GMP compliance and timely results.

The role covers method validation support, SOP and CAPA oversight, cross-functional collaboration, and resource planning. Strong leadership and GMP experience are essential for success in this fast-paced biotech

Qualifications

  • Bachelor’s or Master’s degree in a relevant science field with GMP exposure.
  • Experience leading teams in regulated labs is required.
  • Strong understanding of analytical methods and regulatory expectations in biotech/pharma.

Responsibilities

  • Supervise and schedule the QC Chemistry team to meet testing timelines.
  • Ensure analytical testing of DS/DP/stability samples is GMP compliant.
  • Perform and review physical and chemical analytical methods (HPLC/UPLC/SEC, UV, icIEF, CE-SDS).
  • Serve as primary point of contact and escalation for the team.
  • Lead projects to deliver results and manage lab operations.
  • Review SOPs, change controls, investigations, and CAPAs for the QC Chemistry group.

Skills

Leadership
GMP knowledge
Regulatory awareness
Communication skills
Project management

Education

Bachelor’s in Chemistry, Biochemistry, Biological Sciences, or related science field
Master’s in Chemistry, Biochemistry, Biological Sciences, or related science field

Tools

LIMS
TrackWise
Smartsheet
Kneat validation

Job description

FUJIFILM Biotechnologies seeks a Supervisor, QC Chemistry (First Shift) to lead day-to-day operations in the Chemistry laboratory. You will supervise a team performing routine analytical testing for in-process, DS, DP, and stability samples, ensuring GMP compliance and timely results.

The role covers method validation support, SOP and CAPA oversight, cross-functional collaboration, and resource planning. Strong leadership and GMP experience are essential for success in this fast-paced biotech

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