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Quality Control Internship Jobs (NOW HIRING)

Evonik Corporation

The QC Supervisor is responsible for organizing and directing the daily activities of the Quality ... Train new hires, contractors, and interns while ensuring ongoing procedural compliance for all ...

Evonik Corporation

The QC Supervisor is responsible for organizing and directing the daily activities of the Quality ... Train new hires, contractors, and interns while ensuring ongoing procedural compliance for all ...

CPG Beyond, Inc.

QA/QC Commissioning Associate II

$65K - $97K/yr

TITLE: QA/QC Commissioning Associate II LOCATION: Abernathy, Texas (500 Mile Radius) 75%- 80 ... Experience and/or education and internship in complex facilities or mission critical projects is ...

CPG Beyond, Inc.

QA/QC Commissioning Associate III

$74K - $112K/yr

The QA/QC Commissioning Associate III assists in quality control and quality assurance of data ... Experience and/or education and internship in complex facilities or mission critical projects is ...

CPG Beyond, Inc.

QA/QC Commissioning Associate II

$65K - $97K/yr

The QA/QC Commissioning Associate II assists in quality control and quality assurance of data ... Experience and/or education and internship in complex facilities or mission critical projects is ...

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Quality Control Internship information

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$36K

$81K

$126.5K

How much do quality control internship jobs pay per year?

As of Jul 10, 2026, the average yearly pay for quality control internship in the United States is $81,001.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,000.00 and $97,000.00 per year, depending on experience, location, and employer.

What types of projects or tasks can I expect to work on during a Quality Control Internship?

As a Quality Control Intern, you'll typically assist with inspecting products or materials, conducting laboratory tests, and documenting results to ensure they meet company and regulatory standards. You may help analyze data, support root cause investigations for any defects, and collaborate with production, engineering, or R&D teams to improve processes. Interns often gain hands-on experience with industry-standard equipment and software, and are encouraged to participate in team meetings to understand broader quality initiatives within the organization.

What is the difference between Quality Control Internship vs Quality Assurance Internship?

AspectQuality Control InternshipQuality Assurance Internship
FocusProduct inspection and defect detectionProcess improvement and compliance
CertificationsTypically none required, some may prefer basic quality or industry-specific certificationsSimilar, often no formal certifications required but knowledge of standards helps
Work EnvironmentManufacturing, labs, production linesOffice settings, compliance departments, manufacturing oversight
Industry UsageManufacturing, food, pharmaceuticals, electronicsManufacturing, software, healthcare, engineering

While both internships focus on quality processes, a Quality Control Internship emphasizes inspecting products for defects, whereas a Quality Assurance Internship concentrates on developing and maintaining quality systems and standards. Understanding these differences helps candidates choose the right internship aligned with their career goals in quality management.

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

To thrive as a Quality Control Intern, you generally need a background in science or engineering, attention to detail, and familiarity with quality assurance principles, often gained through relevant coursework or a related degree program. Familiarity with laboratory equipment, data analysis software, and quality management systems like ISO standards is typically expected. Strong analytical thinking, effective communication, and a willingness to learn make an intern stand out. These competencies are crucial for ensuring product consistency, identifying defects, and supporting continuous improvement within the organization.

What is a Quality Control Internship?

A Quality Control Internship is a temporary, entry-level position where students or recent graduates gain hands-on experience in monitoring and ensuring the quality of products or services within a company. Interns typically work under the supervision of quality control professionals, learning to perform inspections, run tests, and document findings. The internship provides valuable exposure to industry standards, quality assurance processes, and regulatory requirements, helping interns develop practical skills for a career in quality management.
More about Quality Control Internship jobs
What cities are hiring for Quality Control Internship jobs? Cities with the most Quality Control Internship job openings:
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Quality Control Internship jobs near you
Infographic showing various Quality Control Internship job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 1% Temporary, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $81,001 per year, or $38.9 per hour.
Senior Scientist I, Quality Control

Senior Scientist I, Quality Control

Candel Therapeutics

Needham, MA • On-site

$155K - $160K/yr

Full-time

Posted 18 days ago

Job description

Salary 155K - $160K + bonus + benefits
On site role in Needham
Senior Scientist I, Quality Control is responsible for executing highly complex analytical assays supporting clinical and commercial programs. This position collaborates with external manufacturing and tech transfer and is focused on Adenovirus and Herpesvirus vectors, associated cell-based potency assays, as well as performing training of new technical staff and troubleshooting and validation of new and established assays. The Senior Scientist I, Quality Control works with various cell lines, performs analytical methods, trends quality attributes, and suitability of product lines for continued use.
Essential Areas of Responsibility:
  • Participate in the development of cell culture and viral vector production using Adenovirus and Herpesvirus production systems.
  • Function as subject matter expert (SME) for technical platforms and new methodologies.
  • Perform assays in support of process development including cell-based assays, ELISA, HPLC, qPCR, SDS-PAGE, UV-spectroscopy.
  • Generate, manage, evaluate, and maintain critical data in a highly organized manner and document in paper or Electronic Laboratory notebook.
  • Participate in the development, optimization, and validation of new assays.
  • Assist with the development of SOPs and batch records for use in Quality Control, or external CMOs.
  • Interact with other departments such as Analytical development, Quality Assurance, Regulatory Affairs, Research, Upstream and Downstream Process Development.
  • Contribute to laboratory support duties associated with operating a QC laboratory.
  • Guide, direct, and train direct reports and team members, including performance monitoring, constructive feedback, quality standards, etc.
  • Able to react to change productively and handle other essential tasks as assigned.

Minimum Education, Experience and Skill Requirements:
Education:
  • PhD or equivalent in biology, chemistry, biochemistry, or related field plus applicable experience. (Internship and/or post-doctoral experience is also accepted)

Experience:
  • Hands-on experience with aseptic techniques related to mammalian cell culture (Vero and HEK293 cells lines)
  • Hands-on experience in laboratory techniques supporting virus, protein and DNA analysis: SDS-PAGE, Western Blot, BCA, residual DNA, HPLC, ELISA.
  • Willingness to learn (new methods, drug development processes, new modalities, etc.) and ability to demonstrate scientific curiosity and innovation.
  • Previous experience in small biotech/pharma company.
  • Previous experience working with viruses.
  • Ability to work independently.
  • Familiarity with basic regulatory expectations around product control strategies and the ICH guidelines for method qualification.
  • Familiarity with Drug Substance and Drug Product release and stability testing programs.
  • A strong background in one or more analytical techniques such as various HPLC based methods, microplate UV/Vis/Luminescent assays, cell-based assays including virus quantification and potency, qPCR, electrophoresis, sizing techniques such as DLS, etc.
  • Ability to write technical documents, including but not limited to method SOPs, development reports, qualification reports, method transfer protocols and method transfer report.
  • Functional understanding of GxP principles.
  • Strong computer skills and good verbal and written communication skills.
  • Very good collaboration and team building skills.

Must be authorized to work in the US. No sponsorships available.
We are not accepting resumes from agencies at this time.

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