Supervisor, QC Chemistry

FUJIFILM Biotechnologies; Holly Springs (NC); On-site; USD 90,000 - 120,000; Full time

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

The Supervisor, QC Chemistry, first shift is responsible for day-to-day supervision, audit readiness, and planning activities for the Chemistry laboratory. This Supervisor will lead a team responsible for performing routine testing of QC analytical chemistry methods used in biological product manufacturing, including chromatography, spectroscopy, electrophoresis, wet chemistry, glycan analysis, peptide mapping, and physical appearance.

What You’ll Do

• Provide supervision and manage scheduling of the QC Chemistry team to ensure testing timelines are achieved.
• Ensure analytical testing of in-process, drug substance (DS), drug product (DP), and stability samples is performed according to appropriate GMP regulations.
• Perform, review, and provide expertise in physical and chemical analytical testing methods, including chromatography (HPLC, UPLC, SEC), spectroscopy (UV, UV-Vis, ELSD), electrophoresis (GE, non-reducing and reducing CE-SDS, imaged capillary isoelectric focusing (icIEF)), wet chemistry, glycan analysis, peptide mapping, and physical appearance per Standard Operating Procedures (SOPs) and test methods.
• Act as primary point of contact for the team and first-line escalation.
• Lead the team to meet project deliverables.
• Set up and maintain operations of a QC testing laboratory.
• Review and approve 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.
• Assist senior management with resource planning and budget-related tasks.
• Gather recommendations for enhancements and gaps; collaborate with leadership to prioritize and implement solutions.
• Liaise with Contract Laboratory Organizations (CLOs) to monitor method execution and the timely delivery of results, as needed.
• Participate in cross-functional collaborations with other QC Departments, Manufacturing, Process Science, and Quality Assurance stakeholders to achieve customer and FUJIFILM Biotechnologies objectives.
• Allocate and plan adequate resources for laboratory testing activities and QA support; provide technical guidance to the team.
• Lead cross-functional teams to achieve operational readiness objectives and new product introduction goals using a risk-based, right-sized approach.
• Lead or guide laboratory staff in investigating deviations/excursions and implementing CAPAs as needed.
• Serve as SME in audits and inspections; prepare and guide the laboratory team to ensure audit readiness.
• Collaborate with the LIMS team and IT department to build new method functionality that meets end-user and customer requirements.
• Establish and maintain internal and external training goals for self and team to ensure compliance with cGMPs and regulatory requirements.
• Provide training, coaching, and mentorship; identify areas for improvement, reduce blind spots, and create growth opportunities aligned to career objectives.
• Perform other duties, as assigned.

Minimum Qualifications

• Bachelor’s in Chemistry, Biochemistry, Biological Sciences, or related science field with 5+ years of experience; OR,
• Master’s in Chemistry, Biochemistry, Biological Sciences, or related science field with 3+ years of experience.
• 2+ years of team management 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.
• Ability to guide and influence teams in a laboratory setting.
• Excellent oral and written communication skills.
• Experience in large pharma/biotech operations or projects.
• Knowledge and experience of physical and chemical analytical testing methods for biological products, including chromatography (GC, HPLC, UPLC, SEC), spectroscopy (MS, GC/MS, LCMS/MS, UV, UV-Vis, FTIR), electrophoresis (GE, non-reducing and reducing CE-SDS, imaged capillary isoelectric focusing (icIEF)), wet chemistry, glycan analysis, peptide mapping, and physical appearance.
• Proven ability to lead teams.

Preferred Qualifications

• Experience managing complex projects.
• 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 preventive action (CAPA), document management system).
• Working knowledge of LIMS, Smartsheet, TrackWise, and/or Kneat validation software.
• Experience and high-level familiarity/understanding of laboratory equipment, utilities qualification, environmental monitoring qualification, quality systems, automation, IT systems, and/or method validation.
• Experience in and thorough understanding of Data Integrity and application of regulatory requirements for QC assays.