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Quality Control Chemist Jobs in Raleigh, NC (NOW HIRING)

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 ...

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 ...

New

Quality Control Analyst

Holly Springs, NC · On-site

$20.75 - $28/hr

Perform raw material compendia chemistry testing for QC samples in a GMP environment. * Perform product chemistry testing for QC samples. * Execute GMP testing and associated tasks in accordance with ...

The Formulation Chemist will also assist QA/QC Chemists in developing testing methodologies and protocols, and work in collaboration with other chemists on the Product Development team. He/she will ...

QC Lead Analyst

Durham, NC

$23.25 - $31.25/hr

QC Lead AnalystPosition Summary The Quality Control (QC) Biochemistry Lead Analyst provides front ... Bachelor's degree highly preferred in Chemistry, Biochemistry, or Biomedical. * Education ...

QC Lead Analyst

Durham, NC

$23.25 - $31.25/hr

QC Lead AnalystPosition Summary The Quality Control (QC) Biochemistry Lead Analyst provides front ... Bachelor's degree highly preferred in Chemistry, Biochemistry, or Biomedical. * Education ...

QC Lead Analyst

Durham, NC · On-site

$23.25 - $31.25/hr

Bachelor's degree highly preferred in Chemistry, Biochemistry, or Biomedical. * Education ... The QC Biochemistry Lead Analyst is a key position in the Biochemistry laboratory performing ...

QC Lead Analyst

Durham, NC · On-site

$23.25 - $31.25/hr

Bachelor's degree highly preferred in Chemistry, Biochemistry, or Biomedical. * Education ... The QC Biochemistry Lead Analyst is a key position in the Biochemistry laboratory performing ...

Chemist A will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. The Chemist will work as a member of team to effectively plan and QC ...

New

Bachelor's degree in chemistry, Biology or related scientific discipline required, advanced degree preferred. * Minimum 12 years of experience in pharmaceutical or biotechnology QC, with. 8 years in ...

Bachelor's degree in chemistry, Biology or related scientific discipline required, advanced degree preferred. * Minimum 12 years of experience in pharmaceutical or biotechnology QC, with. 8 years in ...

Position Overview The Senior, QC Microbiology supports t QC, detecting, and mitigating microbial ... Bachelor's degree in chemistry, Biochemistry, Microbiology or other relevant scientific discipline ...

Senior QC Microbiologist

Holly Springs, NC · On-site

$22 - $29/hr

Position Overview The Senior, QC Microbiology supports t QC, detecting, and mitigating microbial ... Bachelor's degree in chemistry, Biochemistry, Microbiology or other relevant scientific discipline ...

The Senior, QC Microbiology supports t QC, detecting, and mitigating microbial contamination across ... Bachelor's degree in chemistry, Biochemistry, Microbiology or other relevant scientific discipline ...

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Quality Control Chemist information

See Raleigh, NC salary details

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How much do quality control chemist jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for quality control chemist in Raleigh, NC is $30.71, according to ZipRecruiter salary data. Most workers in this role earn between $25.00 and $35.53 per hour, depending on experience, location, and employer.

What are Quality Control Chemists?

Quality Control Chemists are professionals who analyze and test materials and products to ensure they meet required standards and specifications. Their primary responsibility is to conduct laboratory tests on raw materials, in-process samples, and finished products using various chemical and analytical techniques. They document their findings, maintain laboratory equipment, and collaborate with other departments to resolve quality issues. Quality Control Chemists play a vital role in industries such as pharmaceuticals, food and beverage, and manufacturing to ensure product safety and compliance with regulations.

Where do QC chemists work?

Quality Control Chemists typically work in laboratories within manufacturing facilities, pharmaceutical companies, food production plants, or chemical processing plants. They perform testing and analysis of products, often using specialized equipment, and may work standard daytime shifts or in environments requiring strict safety protocols.

What does a quality control chemist do?

A quality control chemist tests and analyzes raw materials, in-process samples, and finished products to ensure they meet quality standards and specifications. They use laboratory equipment and techniques, such as chromatography and spectroscopy, and often follow strict protocols and documentation procedures to maintain product consistency and safety.

What is the highest paying chemist job?

Senior or specialized roles such as Pharmaceutical Chemist, Chemical Research Director, or Quality Control Manager tend to be the highest paying positions for chemists, often earning six-figure salaries. These roles typically require advanced education, extensive experience, and leadership skills in the industry.

How much do QC chemists make in the US?

The average salary for a Quality Control Chemist in the US is around $55,000 to $70,000 per year, depending on experience, education, and location. Entry-level positions typically start lower, while experienced chemists with specialized skills or certifications can earn higher salaries. Many QC chemists also receive benefits such as health insurance and paid time off.

What are the key skills and qualifications needed to thrive as a Quality Control Chemist, and why are they important?

To thrive as a Quality Control Chemist, you need a solid background in chemistry, analytical techniques, and a relevant bachelor's degree in chemistry or a related field. Familiarity with laboratory instruments like HPLC, GC, and spectrophotometers, as well as knowledge of regulatory standards such as GMP or ISO, is typically required. Attention to detail, problem-solving ability, and strong organizational skills are crucial soft skills for this role. These competencies ensure the accuracy, reliability, and compliance of product testing, which are vital for product safety and quality assurance.

What Is a Quality Control Chemist?

A quality control chemist (QC chemist) is a specific type of laboratory chemist, whose primary duties are to measure and test lab materials and products according to industry-specific standard procedures. Jobs are typically in the pharmaceutical or manufacturing fields. As a QC chemist, you assure adherence to all federal regulations and safety procedures. In addition to performing rigorous quality assurance of samples, some QC chemists are responsible for calibrating and performing maintenance on lab equipment. Relevant qualifications for this career include a bachelor’s degree in chemistry, experience in a chemistry lab setting, and skills like attention to detail and the ability to multitask.

What is the difference between Quality Control Chemist vs Quality Assurance Technician?

AspectQuality Control ChemistQuality Assurance Technician
CredentialsBachelor's in Chemistry or related field; certifications like CQE beneficialBachelor's in Chemistry, Quality Management, or related; certifications like CQTA helpful
Work EnvironmentLaboratory setting, testing raw materials, in-process, and finished productsManufacturing or production environment, focusing on process compliance and documentation
Employer & IndustryPharmaceutical, food, cosmetics, chemical industriesManufacturing, pharmaceutical, food, and beverage industries

While both roles ensure product quality, the Quality Control Chemist primarily conducts laboratory testing and analysis, whereas the Quality Assurance Technician focuses on process monitoring and compliance to prevent defects. Both positions are essential for maintaining product standards in manufacturing industries.

What are some common challenges faced by Quality Control Chemists in maintaining consistent testing standards across different production batches?

Quality Control Chemists often encounter challenges in ensuring consistency due to variations in raw materials, equipment calibration, and environmental conditions. Addressing these issues requires diligent documentation, regular equipment maintenance, and strict adherence to standard operating procedures. Effective communication with production and R&D teams is also essential to quickly resolve discrepancies and implement corrective actions, ensuring that all products meet quality and regulatory standards.
What are popular job titles related to Quality Control Chemist jobs in Raleigh, NC? For Quality Control Chemist jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Quality Control Chemist jobs in Raleigh, NC look for? The top searched job categories for Quality Control Chemist jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Quality Control Chemist jobs? Cities near Raleigh, NC with the most Quality Control Chemist job openings:
Infographic showing various Quality Control Chemist job openings in Raleigh, NC as of July 2026, with employment types broken down into 77% Full Time, and 23% Contract. Highlights an 100% In-person job distribution, with an average salary of $63,875 per year, or $30.7 per hour.
Supervisor, QC Chemistry

Supervisor, QC Chemistry

Fujifilm

Holly Springs, NC

Full-time

Posted 2 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 535 rated manufacturers


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.


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


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.


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.


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).


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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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