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Fujifilm

Global precision manufacturer for healthcare

Lead QC Associate 2

Inspection & TestPosted on Nov 5
Full-timeResearch Triangle Park, Durham, NC, USANo salary listedIn-person

About the Job

Requirements

  • A Bachelor of Science or Bachelor of Arts, preferably in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related technical field, and at least 2 years of direct experience.
  • Strong experience with high-performance liquid chromatography (HPLC).
  • Ability to work in environments that may necessitate respiratory protection.
  • Ability to discern audible cues.
  • Ability to inspect or perform tasks with 20/20 corrected vision and visual acuity, including distinguishing color.
  • Ability to ascend or descend ladders, scaffolding, and ramps.
  • Ability to stand and sit for prolonged periods of up to 240 minutes.
  • Ability to conduct activities using repetitive motions involving the wrists, hands, and/or fingers.
  • Ability to move objects up to 33 pounds.
  • Ability to bend, push or pull, reach to retrieve materials from 18 to 60 inches in height, and use twisting motions.
  • Ability to work in warm or cold environments ranging from 0 to 100°F.

Responsibilities

  • Perform a broad range of assigned laboratory support functions and procedures, demonstrating expertise in technical skills, disciplines, and procedures within assigned discipline areas.
  • Serve as a subject matter expert responsible for corrective and preventive actions, audit actions, deviations, laboratory investigations, method revisions, and other related Quality System activities.
  • Lead problem-solving and troubleshooting and recommend mitigation and process improvements.
  • Support laboratory and assay functions, including housekeeping, safety, logbook use and maintenance, equipment use and maintenance, method execution, and data review.
  • Lead method transfers, method validations, and method qualification as a subject matter expert.
  • Apply lean laboratory and Six Sigma principles to laboratory processes.
  • Review technical data; provide expert review and input on new methods and revisions; create data reviews and summary reports; and interpret data.
  • Notify management and initiate events, such as deviations, in the quality systems.
  • Prioritize and organize work to meet established schedules and deadlines; coordinate laboratory testing or supporting documentation logistics with others in the group as needed.
  • Prepare technical writing, such as reports and deviation initiations, using pre-existing templates as needed.
  • Meet schedules with right-first-time results and high-quality effort, taking initiative to communicate, coordinate, and adjust work efforts to achieve these objectives.
  • Assist with deviations, laboratory investigations, procedure changes, and method transfer planning.
  • Undertake assigned project responsibilities, such as department representation, document development or review, troubleshooting, and protocol execution.
  • Contribute to team goals and teamwork within the unit and across the department.
  • Identify and solve problems while informing and consulting with area management.
  • Assess data holistically in the context of validity, reliability, and impact relative to the batch at hand and other related batches and processes.
  • Perform or lead laboratory investigations, identify deviations, and implement corrective actions.

Desired Qualifications

  • Experience with compendial analysis, United States Pharmacopeia (USP), European Pharmacopoeia (EP), and Japanese Pharmacopoeia (JP), method validation or verification, Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, Karl Fischer titration, polarimetry, and refractometry.
  • Previous experience with TrackWise and deviation writing.

About the Company

Fujifilm

Global precision manufacturer for healthcare

Fujifilm is the main operating and manufacturing arm of the Fujifilm group, turning precision chemistry, nanotechnology, and optical engineering from the film era into products for deep tech and life sciences. It runs Bio CDMO facilities that manufacture complex biopharmaceuticals and vaccines, and its materials division makes photoresists and chemical slurries essential to semiconductor and display production. In healthcare, it develops AI-powered imaging devices, endoscopes, and ultrasound systems, while also serving consumers with INSTAX instant photos and X-Series cameras. Its goal is to translate core technical capabilities into reliable, market-ready products across healthcare, electronics materials, and imaging, maintaining leadership in precision manufacturing and applied science.

Company size
501-1,000
Company stage
IPO
Headquarters
Tokyo, Japan
Founded
1934

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