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Internship Pharmaceutical Quality Control Jobs (NOW HIRING)

Actalent

**QC Scientist I**

Saint Louis, MO

$28 - $31/hr

Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Biology, Biotechnology, or a ... industry experience, internships, co-ops, research, or laboratory coursework. * Strong ...

Actalent

QC Scientist I

Saint Louis, MO

$28 - $31/hr

Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Biology, Biotechnology, or a ... industry experience, internships, co-ops, research, or laboratory coursework. * Strong ...

Socket.dev

Pharmaceutical QA Director

Tustin, CA · On-site

$180 - $260/hr

Demonstrated expertise in departmental leadership, quality control, microbiology quality assurance, and process quality assurance within a pharmaceutical manufacturing environment. * Strong knowledge ...

New

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 ...

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 ...

KVK Tech

Be Seen First

QC Chemist I/II

Newtown, PA · On-site

$56K - $90K/yr

S.-based generic and specialty pharmaceutical manufacturer committed to developing and producing ... What You'll Do The QC Chemist I/II performs analytical testing of raw materials, in-process ...

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 ...

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Internship Pharmaceutical Quality Control information

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 are the typical responsibilities of an internship 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 are the key skills and qualifications needed for an internship in pharmaceutical quality control?

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.

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.

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What are the most commonly searched types of Pharmaceutical Quality Control jobs?

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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 August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution.

Pharmaceutical Quality Control Associate

Norwood, MA

Randstad
Recruiting and Staffing Services • 5 - 10K employees
Learn more about Randstadexternal

$41 - $42/hr

Full-time

Posted 6 days ago

Job description

Ready to Make an Impact in Biotech Quality Control?

Join a high-performing team dedicated to advancing life-saving therapies! We are seeking a detail-oriented Quality Control Associate II to support cGMP QC testing for raw materials, drug substances, and finished products at our state-of-the-art manufacturing facility.

In this hands-on, on-site role, you will execute and troubleshoot core analytical methods, drive method transfers, and ensure absolute compliance with cGMP standards. If you excel in a fast-paced environment and want to apply your testing expertise directly to patient safety, this opportunity is for you!

The Role The Quality Control Associate II will support cGMP QC testing for raw materials, drug substances, and finished products at the company's manufacturing facility and affiliated contract organizations. This role includes executing and troubleshooting analytical methods, supporting method transfers, qualification activities, and ensuring compliance with cGMP standards. This is an on-site position.Here’s What You’ll Need (Basic Qualifications) Education: BA/BS DegreeExperience: STEM degree with 3-5 years’ of experience in a cGMP laboratory setting, with hands-on experience in mammalian cell culture, cell based and potency assays, ELISA, molecular biology, and Protein Analysis.Here’s What You’ll Bring to the Table (Preferred Qualifications)
  • Method development/qualification experience with molecular biology, cell-based assays, or protein analysis methods.
  • Trained in Aseptic techniques and general laboratory instrumentation (e.g. pH meters, balances, pipettes)
  • Ability to prepare reagents, pipette small volumes, work in a Biological Safety Cabinet
  • Experience with laboratory equipment calibration and maintenance.
  • Ability to work effectively in a fast-paced, cross-functional matrix environment.
  • Familiarity with relevant FDA, EU, ICH guidelines, and regulations.
INTERESTED? APPLY NOW! THESE POSITIONS FILL FAST! salary: $41 - $42 per hour
shift: First
work hours: 8 AM - 5 PM
education: Bachelors

Responsibilities

  • Execute QC molecular biology and Bioassay methods (e.g. Mammalian cell based potency, qPCR, sequencing, protein analysis)
  • Assist in troubleshooting equipment and assay issues.
  • Perform general laboratory support activities including reagent preparation, equipment maintenance, housekeeping, logbook reviews, etc.
  • Establish and maintain a safe laboratory working environment.
  • Write, revise, and maintain SOPs, protocols, and reports.
  • Support training as assigned.
  • Assist in execution of Quality records (i.e. investigations, change controls, CAPAs)
  • Ensure compliance with cGMP documentation and regulatory guidelines.
  • Accountable for all mandatory training and assigned tasks.
  • Provide support during audits and collaborate on continuous improvement initiatives.
  • Additional duties may be assigned.

Skills
  • Quality Control
  • Quality Assurance
  • cGMP
  • GMP
  • raw materials
  • Drug Substance
  • ELISA (1 year of experience is required)
  • mammalian cell culture
  • cell based and potency assays
  • molecular biology

    • Qualifications
  • Years of experience: 2 years
  • Experience level: Experienced

    • Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.


    Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
    At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
    Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
    This posting is open for thirty (30) days.
    It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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About Randstad USA

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Our business is supporting business productivity, from matching the right people with great jobs to custom project solutions and consulting. We use innovative technologies and a passion for people to provide you with the best experience possible. We provide outsourcing, staffing, consulting and workforce solutions within the areas of engineering, accounting and finance, healthcare, human resources, IT, legal, life sciences, manufacturing and logistics, office and administration and sales and marketing. We can’t wait to tell you all about it.

Industry

Recruiting and staffing services

Company size

5,001 - 10,000 Employees

Headquarters location

Minneapolis, MN, US

View All Randstad USA Jobs