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Quality Control Chemistry Intern Jobs (NOW HIRING)

INCOG

Associate QC Chemist, 3rd Shift

Fishers, IN · On-site

Bachelor's Degree in Science (Chemistry or Biochemistry) * Minimum of 3+ years of biopharma industry experience, with at least 2 years of hands-on experience in a GMP environment/Quality Control ...

FUJIFILM Biotechnologies

The Senior Analyst 1, QC Chemistry, adheres to GMP-compliant laboratory operations in accordance with regulatory guidelines. This role generates analytical results and identifies laboratory ...

Cardinal Health, Inc.

$90 - $115/hr

What a Supervisor, Quality Control (Chemistry) contributes to Cardinal Health Quality Control is responsible for the analysis and inspection of products or processes for compliance with ...

Alcami-5

Scientist I - QC Chemistry

Wilmington, NC · On-site

$65 - $85/hr

Job Summary The Scientist I - QC Chemistry is accountable for driving results in a fast-paced environment by performing analytical routine testing in support of pharmaceutical product development or ...

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How much do quality control chemistry intern jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for quality control chemistry intern in the United States is $18.67, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $17.31 per hour, depending on experience, location, and employer.

What does a quality control chemistry intern do?

A Quality Control Chemistry Intern assists in testing and analyzing raw materials, in-process samples, and finished products to ensure they meet quality and safety standards. They work under the supervision of experienced chemists, using various laboratory instruments and techniques such as titration, spectroscopy, and chromatography. Interns are also responsible for maintaining accurate records of test results, following strict lab procedures, and helping to troubleshoot issues with equipment or processes. This role provides valuable hands-on experience in a laboratory environment and helps interns develop skills important for a career in quality control and analytical chemistry.

What are the key skills and qualifications needed to thrive as a quality control chemistry intern?

To thrive as a Quality Control Chemistry Intern, you need a solid understanding of analytical chemistry, laboratory safety, and experience with standard laboratory procedures, typically gained through coursework in chemistry or a related science. Familiarity with analytical instruments such as HPLC, GC, and spectrophotometers, as well as proficiency in using laboratory information management systems (LIMS), is often required. Attention to detail, strong organizational skills, and effective communication are crucial soft skills for accurately documenting data and collaborating with team members. These skills and qualities ensure precise testing, regulatory compliance, and support the overall quality assurance process in laboratory environments.

What types of projects or tasks can a quality control chemistry intern expect to work on during their internship?

As a Quality Control Chemistry Intern, you can expect to be involved in hands-on laboratory work such as preparing chemical solutions, conducting routine analytical tests like HPLC or titrations, and supporting the documentation of results in accordance with Good Laboratory Practices (GLP). You may also assist with equipment calibration, participate in investigations of out-of-specification results, and help maintain lab safety and cleanliness. This role often requires close collaboration with experienced chemists and quality assurance teams, offering valuable exposure to industry-standard procedures and teamwork within a regulated environment.

What is the difference between Quality Control Chemistry Intern vs Quality Control Chemist?

AspectQuality Control Chemistry InternQuality Control Chemist
CredentialsEnrolled in or recent graduate of a chemistry or related programBachelor's degree in chemistry or related field, often with experience
Work EnvironmentLaboratory, internship setting, supervisedLaboratory, production, or quality assurance departments, more autonomous
Employer & Industry UsageInternship programs in pharmaceutical, biotech, or manufacturing companiesFull-time roles in similar industries, responsible for quality testing

The main difference is that a Quality Control Chemistry Intern is typically a student or recent graduate gaining hands-on experience under supervision, while a Quality Control Chemist is a full-time professional responsible for routine testing and quality assurance tasks. Interns focus on learning, whereas Chemists perform ongoing quality control duties independently.

What cities are hiring for Quality Control Chemistry Intern jobs?

Cities with the most Quality Control Chemistry Intern job openings:

What states have the most Quality Control Chemistry Intern jobs?

States with the most job openings for Quality Control Chemistry Intern jobs include:

Quality Control Chemistry Intern jobs near you
Infographic showing various Quality Control Chemistry Intern job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $38,842 per year, or $18.7 per hour.

Senior Analyst 1, QC Chemistry

Fujifilm

Holly Springs, NC • On-site

Other

Re-posted 11 days ago

Fujifilm rating

8.5

Company rating: 8.5 out of 10

Based on 70 frontline employees who took The Breakroom Quiz

33rd of 545 rated manufacturers

Job description

Position Overview
The Senior Analyst 1, QC Chemistry works with limited direction to execute QC Analytical Chemistry methods used in biological product manufacturing, including chromatography, spectroscopy, electrophoresis, wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance, etc. The Senior Analyst 1, QC Chemistry, adheres to GMP-compliant laboratory operations in accordance with regulatory guidelines. This role generates analytical results and identifies laboratory exceptions, invalid assays, deviations, change controls, and corrective and preventative actions (CAPAs). The Senior Analyst 1, QC Chemistry is primarily responsible for executing routine analytical methods in support of manufacturing, supporting laboratory execution of analytical method transfers and validations, and training other QC Chemistry laboratory associates.
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
  • Executes physical and chemical analytical testing methods used in biological product manufacturing, including chromatography (GC, HPLC, UPLC, SEC), spectroscopy (MS, GC/MS, LC-MS/MS, UV, UV-Vis, FTIR), electrophoresis (GE, non-reducing and reducing CE-SDS, imaged capillary isoelectric focusing (icIEF)), wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance, etc.
  • Ensures analytical testing of in-process, drug substance (DS), drug product (DP), and stability samples is performed according to appropriate GMP regulations.
  • Ensures analytical testing data is captured in LIMS software and data integrity is maintained.
  • Reports assay performance and assists with implementing improvements that ensure quality and efficiency within QC Chemistry.
  • Identifies and follows up on excursions and deviations and initiates corrective and preventative actions (CAPAs).
  • Coordinates and supports QC Chemistry lab activities as needed.
  • Provides training for QC Chemistry lab associates.
  • Authors and reviews SOPs and technical reports.
  • Works cross-functionally with other QC departments, Manufacturing, Process Science, and Quality Assurance stakeholders to achieve customer and FUJIFILM Biotechnologies objectives.
  • Performs other duties, as assigned.

Minimum Qualifications
  • Bachelor's Degree in Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field with 3+ years of experience 1- 3 years relevant experience.
  • 3+ years laboratory experience.
  • 1-3 years GMP laboratory experience.
  • Experience with physical and chemical analytical testing methods used in biological product manufacturing including chromatography (GC, HPLC, UPLC, SEC), spectroscopy (MS, GC/MS, LC-MS/MS, UV, UV-Vis, FTIR), electrophoresis (GE, non-reducing and reducing CESDS, imaged capillary isoelectric focusing (icIEF)), wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance, etc.. with cellular and molecular analytical testing methods

Preferred Qualifications
  • Master's Degree in Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field.
  • 1+ years of experience with Raw Material methodology as it pertains to cGMP.
  • Experience with LIMS software.

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.
*LI-Onsite
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).

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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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