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Internship Pharmaceutical Quality Control Jobs (NOW HIRING)

Garonit Pharmaceutical

QC Supervisor

Fairfield, NJ · On-site

Bachelor's degree in Chemistry or a related scientific field. * 2+ years in a supervisory or management role in a pharmaceutical QC lab. * Strong experience with Empower 3, HPLC, GC, and wet ...

Garonit Pharmaceutical

QC Supervisor

Fairfield, NJ · On-site

Bachelor's degree in Chemistry or a related scientific field. * 2+ years in a supervisory or management role in a pharmaceutical QC lab. * Strong experience with Empower 3, HPLC, GC, and wet ...

Astrix Inc

QC Analyst II (Chemistry)

Rensselaer, NY · On-site

$30 - $47/hr

Candidates with strong analytical chemistry, chromatography, and pharmaceutical QC laboratory experience are highly encouraged to apply. Key Responsibilities * Perform analytical testing for incoming ...

Cipla

Quality Control (QC) Chemist

Fall River, MA

$65K - $105K/yr

Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems) * Evaluate critical quality attributes (CQA) such as particle ...

ANI Pharmaceuticals

Quality Control Technician

Baudette, MN · On-site

$17.25 - $22/hr

Position Summary Responsible for supporting Quality Control testing operations through laboratory ... Zero to two years of experience in a laboratory or pharmaceutical environment preferred. * Ability ...

ANI Pharmaceuticals

Quality Control Technician

Baudette, MN · On-site

$17.25 - $22/hr

Position Summary Responsible for supporting Quality Control testing operations through laboratory ... Zero to two years of experience in a laboratory or pharmaceutical environment preferred. * Ability ...

Cipla

Quality Control (QC) Chemist

Fall River, MA · On-site

$65K - $105K/yr

Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems) * Evaluate critical quality attributes (CQA) such as particle ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

Adecco

QC Scientist I

Cincinnati, OH

$25/hr

QC Scientist I Location: Cincinnati, OH Pay Rate: $ 25.00/hour Position Summary We are seeking a ... Conduct pharmaceutical residual testing utilizing HPLC, Mass Spectrometry, and Total Organic Carbon ...

System One Holdings, LLC

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

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Internship Pharmaceutical Quality Control information

What are some typical responsibilities for interns in Pharmaceutical Quality Control?

As a Pharmaceutical Quality Control intern, you can expect to assist with routine laboratory testing of raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with regulatory standards. Responsibilities often include preparing chemical reagents, performing analytical techniques (such as HPLC or spectroscopy) under supervision, recording and analyzing data, and maintaining lab equipment. Interns also learn proper documentation practices and may support investigations of deviations or out-of-specification results. This hands-on experience provides insight into the strict quality standards and teamwork required in the pharmaceutical industry.

What is an Internship in Pharmaceutical Quality Control?

An Internship in Pharmaceutical Quality Control is a temporary training position where students or recent graduates gain practical experience in ensuring the quality and safety of pharmaceutical products. Interns typically work in laboratory settings, assisting with sample analysis, documentation, equipment calibration, and compliance with regulatory standards. This role helps interns develop key skills in laboratory techniques, data analysis, and understanding of Good Manufacturing Practices (GMP). It is a valuable opportunity for those considering a career in the pharmaceutical or biotechnology industries.

What is the difference between Internship Pharmaceutical Quality Control vs Pharmaceutical Quality Control Analyst?

AspectInternship Pharmaceutical Quality ControlPharmaceutical Quality Control Analyst
QualificationsEnrolled in or recent graduate of related degreeBachelor's degree in pharmacy, chemistry, or related field
Work EnvironmentTraining-focused, supervised lab settingFull-time professional lab environment
ResponsibilitiesAssisting with tests, learning proceduresPerforming quality tests, data analysis

Internship Pharmaceutical Quality Control roles are entry-level positions designed for students or recent graduates to gain industry experience. In contrast, Pharmaceutical Quality Control Analysts are full-time professionals responsible for executing quality tests and ensuring product compliance. The internship provides foundational exposure, while the analyst role involves independent work and responsibility.

What are the key skills and qualifications needed to thrive as an Internship Pharmaceutical Quality Control, and why are they important?

To excel in a Pharmaceutical Quality Control internship, you need a solid understanding of chemistry, laboratory procedures, and basic GMP regulations, often gained through relevant coursework or a degree in pharmacy, chemistry, or a related field. Familiarity with analytical instruments like HPLC, GC, and software for data analysis is highly valued. Attention to detail, strong organizational skills, and effective communication set candidates apart in this environment. These skills ensure the accuracy and reliability of product testing, which is critical for maintaining safety, regulatory compliance, and product quality.
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Internship Pharmaceutical Quality Control jobs near you
Infographic showing various Internship Pharmaceutical Quality Control job openings in the United States as of July 2026, with employment types broken down into 66% Full Time, 17% Part Time, and 17% Contract. Highlights an 100% In-person job distribution.
QC Supervisor

QC Supervisor

Garonit Pharmaceutical

Fairfield, NJ • On-site

Other

Posted 18 days ago

Job description

QC Supervisor

Onsite in Fairfield, NJ

We're looking for a QC Supervisor who's both a hands-on technical expert and a strong leader. This role manages the daily operations of our QC Laboratory - leading testing, method development, and data review while ensuring full cGMP compliance.

 What You'll Do

  • Supervise and lead a team of QC chemists and analysts.
  • Oversee all analytical testing for manufacturing, release, and stability.
  • Review and interpret HPLC, GC, and wet chemistry data in compliance with cGMP.
  • Author and review SOPs, analytical methods, and validation protocols.
  • Conduct and support laboratory investigations, CAPA, and change controls.
  • Manage and schedule lab workloads to meet production timelines.
  • Ensure lab safety, data integrity, and adherence to FDA and ICH guidelines.
  • Collaborate cross-functionally to resolve quality-related issues quickly.
  • Develop and mentor QC staff through training and performance development.
  • Support continuous improvement initiatives to enhance compliance and efficiency.

 What You'll Bring

  • Bachelor's degree in Chemistry or a related scientific field.
  • 2+ years in a supervisory or management role in a pharmaceutical QC lab.
  • Strong experience with Empower 3, HPLC, GC, and wet chemistry.
  • Deep understanding of cGMP, ICH, CFR, and USP testing requirements.
  • Experience in method development, validation, and stability testing.
  • Proven leadership, training, and coaching skills.
  • Excellent problem-solving, documentation, and communication abilities.
  • High attention to detail, strong work ethic, and commitment to quality.

 Why Garonit Pharma

  • Work with cutting-edge equipment in a collaborative, growth-oriented environment.
  • Play a key role in ensuring product quality and regulatory success.
  • Competitive compensation and career growth opportunities.

Apply