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Quality Control Lab Assistant Jobs in Raleigh, NC

Coordinates and supports QC Chemistry lab activities as needed. * Works cross-functionally with other QC departments, Manufacturing, Process Science, and Quality Assurance stakeholders to achieve ...

Coordinates and supports QC Chemistry lab activities as needed. * Works cross-functionally with other QC departments, Manufacturing, Process Science, and Quality Assurance stakeholders to achieve ...

Manage the site QC Lab. Conduct routine and non-routine QC testing. Maintain all lab supplies for the main QC lab and the production QC labs. Responsible for the Quality Analysts who reports to the ...

The main function of the Associate Specialist, Quality Control is to assist in the assurance of the quality of product through the performance of microbiological, chemical and analytical sampling and ...

Manage the site QC Lab. Conduct routine and non-routine QC testing. Maintain all lab supplies for the main QC lab and the production QC labs. Responsible for the Quality Analysts who reports to the ...

Manage the site QC Lab. Conduct routine and non-routine QC testing. Maintain all lab supplies for the main QC lab and the production QC labs. Responsible for the Quality Analysts who reports to the ...

Position Summary - The Quality Control Raw Materials Chemist I performs testing using a variety of ... Create purchase requisitions for lab supplies and third-party testing * Perform weekly laboratory ...

QA/QC Solar Technician

Raleigh, NC

$18.25 - $23.25/hr

The Role Cypress Creek Energy is seeking a highly motivated QA/QC Solar Technician with utility ... Conduct on-site inspections and evaluations of solar photovoltaic facilities. * Assist in planning ...

Position Summary - The Quality Control Raw Materials Chemist I performs testing using a variety of ... Create purchase requisitions for lab supplies and third-party testing * Perform weekly laboratory ...

Showing results 41-60

Quality Control Lab Assistant information

See Raleigh, NC salary details

$11

$22

$39

How much do quality control lab assistant jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for quality control lab assistant in Raleigh, NC is $22.20, according to ZipRecruiter salary data. Most workers in this role earn between $15.87 and $22.45 per hour, depending on experience, location, and employer.

What is the difference between Quality Control Lab Assistant vs Quality Control Technician?

AspectQuality Control Lab AssistantQuality Control Technician
CredentialsHigh school diploma or equivalent; certifications varyHigh school diploma; often additional certifications or training
Work EnvironmentLaboratory setting, supporting testing activitiesLaboratory and production environments, performing tests and inspections
Job ResponsibilitiesAssisting with sample preparation and data entryConducting tests, analyzing results, and ensuring quality standards

While both roles work in laboratory settings within quality assurance, the Quality Control Lab Assistant primarily supports testing processes and data management, whereas the Quality Control Technician actively performs testing and analysis to ensure product quality. The Technician role typically requires more technical skills and certifications, making it more hands-on in quality control procedures.

What are the key skills and qualifications needed to thrive as a quality control lab assistant, and why are they important?

To thrive as a Quality Control Lab Assistant, you need a background in chemistry or biology, attention to detail, and familiarity with laboratory procedures, often supported by an associate's degree or relevant coursework. Experience using analytical instruments such as spectrophotometers, pH meters, and laboratory information management systems (LIMS) is typically required. Strong organizational skills, effective communication, and the ability to follow precise protocols help set top performers apart. These skills and qualities are crucial to ensuring accurate testing, regulatory compliance, and the overall reliability of laboratory results.

What does a quality control lab assistant do?

A Quality Control Lab Assistant supports laboratory operations by conducting tests and inspections on products or materials to ensure they meet specified standards. They prepare samples, operate laboratory equipment, record and analyze data, and help maintain a clean and organized lab environment. Their work helps identify defects or deviations from quality standards, contributing to the overall safety and effectiveness of products before they reach customers.

What are some common challenges faced by quality control lab assistants, and how can they be managed?

Quality Control Lab Assistants often face challenges such as maintaining strict adherence to standardized testing protocols, managing a high volume of samples under tight deadlines, and ensuring accurate record-keeping for compliance purposes. To manage these challenges, it's important to develop strong organizational skills, attention to detail, and effective communication with team members and supervisors. Many labs provide thorough training and encourage collaboration, which helps new assistants acclimate to the fast-paced environment while maintaining high-quality standards.
What cities near Raleigh, NC are hiring for Quality Control Lab Assistant jobs? Cities near Raleigh, NC with the most Quality Control Lab Assistant job openings:

Supervisor, QC Chemistry

Fujifilm

Holly Springs, NC

Full-time

Posted 15 days ago


Fujifilm rating

8.4

Company rating: 8.4 out of 10

Based on 67 frontline employees who took The Breakroom Quiz

50th of 537 rated manufacturers


Job description

Position Overview

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.

Company Overview

FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.

We're looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we're proud to cultivate a culture that will fuel your purpose, energy, and drive-what we call Genki. Ready to shape the future of medicine? Let's transform healthcare together!

Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh's thriving tech scene, making it the perfect blend of community and opportunity.

Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: https://www.fujifilm.com/us/en/about/region/careers

Job Description

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.

Physical Requirements:

The physical demands described here are representative of those that must be met by an employee to

successfully perform the essential functions of this job. Reasonable accommodations may be made to

enable individuals with disabilities to perform essential functions. While performing the duties of this job,

the employee is required on a regular basis to:

  • Ability to discern audible cues.
  • Ability to inspect or perform a task with 20/20 corrected vision, visual acuity, including distinguishing color.
  • Ability to stand for prolonged periods of time up to 240 minutes.
  • Ability to sit for prolonged periods of time up to 240 minutes.
  • Ability to conduct activities using repetitive motions that include wrist, hands and/or fingers.
  • Ability to conduct work that includes moving objects up to 10 pounds.
  • Ability to bend, push or pull, and reach to retrieve materials from 18" to 60" in height, and use twisting motions.
  • Will work in warm/cold environments.
  • Will work in small and/or enclosed spaces.

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.

EEO Information

Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.

ADA Information

If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBN_PNC@fujifilm.com).

Employment Type: OTHER

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About Fujifilm

Sourced by ZipRecruiter

With each Industry we enter, We’ve learned to Leverage and Adapt our knowledge, Expertise and rRsources to make the World a better place. When it comes to Innovating for a Healthier World and a more sustainable society, we’ll NEVER STOP. Fujifilm will contribute to the social challenges by creating new value in a wide range of business domains through innovation in Products, Services, and Technological Development. We launched our Healthcare Business with X-ray film in 1936. And now, We are developing our business in areas of prevention, diagnosis, and treatment as a Comprehensive Healthcare Company. We will never stop Innovating for a Healthier World.

Industry

Chemical manufacturing

Company size

10,000+ Employees

Headquarters location

Minato-ku, Tokyo, JP

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