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Quality Control Chemistry Intern Jobs (NOW HIRING)

Guerbet

QC Chemistry Lead

Raleigh, IL

QC Chemistry Lead At Guerbet, we build lasting relationships so that to enable people to live better . This is Our Purpose. We are a global leader in medical imaging, offering an extensive portfolio ...

Laboratoire Guerbet

QC Chemistry Lead

Raleigh, IL · On-site

QC Chemistry Lead At Guerbet, we build lasting relationships so that to enable people to live better . This is Our Purpose. We are a global leader in medical imaging, offering an extensive portfolio ...

Novartis

Supervisor, QC Chemistry

Indianapolis, IN · On-site

$88K - $132K/yr

In this people management role, the QC Chemistry Supervisor works with the Quality Control team in supporting our efforts of RLT therapy. This role is responsible for the day-to-day oversight of the ...

NEPHRON SC, LLC

QC Chemistry Technician

West Columbia, SC · On-site

$18 - $22.75/hr

The QC Chemistry Technician is responsible for performing routine chemical testing, sample preparation, instrument operation, and documentation to support quality control activities in accordance ...

INCOG

QC Chemist, 3rd Shift

Fishers, IN

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 ...

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Quality Control Chemistry Intern information

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

As of Jul 6, 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 jobs can I get with a chemistry minor?

A chemistry minor can qualify you for roles such as Quality Control Chemistry Intern, laboratory technician, research assistant, or quality assurance associate. These positions often require knowledge of laboratory techniques, data analysis, and familiarity with scientific tools and safety protocols.

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.

Where do QC chemists work?

QC chemists typically work in laboratories within manufacturing facilities, pharmaceutical companies, food production plants, or chemical processing plants. They perform testing and analysis of products to ensure quality standards are met, often using tools like spectrometers and chromatography equipment, and may work regular business hours or shifts depending on the industry.

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

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 can you do with a graduate degree in chemistry?

A graduate degree in chemistry can lead to roles such as a Quality Control Chemistry Intern, where you perform laboratory testing, analyze data, and ensure product quality. It also opens opportunities in research and development, regulatory compliance, and analytical chemistry, often requiring skills in laboratory techniques and familiarity with scientific software.

What jobs can a chemistry graduate get?

A chemistry graduate can pursue roles such as Quality Control Chemistry Intern, laboratory technician, research associate, or analytical chemist. These positions often require knowledge of laboratory techniques, data analysis, and familiarity with scientific tools and safety protocols.

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 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
Manager, Quality Control Chemistry

Manager, Quality Control Chemistry

BeiGene, Inc.

Pennington, NJ • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 17 days ago

Job description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:
Manages all Quality Control (QC) Chemistry Laboratory - Capillary Electrophoresis (CE) activities to support GMP manufacturing, testing and release of materials, intermediates, and finished products under FDA/EU regulations, applicable International Regulations, BeOne processes and procedures. Establishes and implements QC Chemistry procedures including but not limited to capillary electrophoresis and supports regulatory compliance inspections. Ensures efficient and effective day-to-day operations of the CE laboratory. This position reports to the Senior Manager QC and is located full-time at the Hopewell, NJ site.
Essential Functions of the Job:
  • Lead the QC Chemistry (CE) laboratory daily workflow.
  • Establish and maintain QC Chemistry (CE) laboratory related quality systems to ensure conformance with regulations and BeOne Global quality standards.
  • Manage QC Chemistry (CE) laboratory routine operations, including but not limited to validation, SOPs, specifications, testing records, personnel training and assessment, scheduling, etc.
  • Ensure QC Chemistry (CE) laboratory compliance with Environmental Health and Safety (EHS) standards.
  • Ensure timely completion of testing (e.g., In-process control, DS release, DP release, and stability testing) to ensure timely generation and reporting of test results in support of manufacturing operations.
  • Review of laboratory test results, ensuring adherence to Good Documentation Practices.
  • Ensure appropriate investigation of OOS events, discrepancies, lab errors, and equipment failures.
  • Implementation of effective corrective actions and preventive actions (CAPAs).
  • Participate in internal and external GMP audits where possible.
  • Ensure that the QC Chemistry (CE) laboratory meets or improves on budget, cost, volume, and efficiency targets (KPIs) in line with business objectives.
  • Expertise in Quality Control (QC) within a Good Manufacturing Practice (GMP) environment, ensuring compliance with industry standards and regulations through hands-on laboratory experience.
  • Working knowledge and experience with capillary electrophoretic analytical methods such as reduced and non-reduced CGE, CZE, and cIEF/icIEF, etc.
  • Knowledgeable with USP/EP and cGMP/EU GMP regulations.
  • Familiar with instrument and equipment validation.
  • Expert knowledge of quality control principles, practices and standards for the biopharmaceutical industry.
  • Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level.
  • Strong leadership/team management skills and experience.
  • Manage, motivate, coach and mentor direct reports.
  • Credible and confident communicator (written and verbal) at all levels.
  • Strong analytical, problem-solving ability, with excellent attention to detail, with the ability to work accurately in a busy and demanding environment.
  • Excellent project management skills.
  • Hands-on approach, with a 'can do' attitude.
  • Ability to prioritize, demonstrating good time management skills.
  • Self-motivated, with the ability to work proactively using own initiative.
  • Committed to learning and development.
  • Interacts with all levels of BeOne employees
  • Undertake any other duties as required

Supervisory Responsibilities:
  • Manage direct reports from QC Chemistry (CE) laboratory
  • 2+ years of managerial experience directly managing people required
  • Leadership experience leading teams, projects, programs or directing the allocation of resources.

Computer Skills:
  • Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint).
  • Ability to work on a computer for extended periods of time

Travel:
  • Must be willing to travel approximately 10%

Education Required:
  • Bachelor's Degree in Chemistry, Biochemistry, or Biotechnology related scientific discipline with 5+ years of GMP testing using capillary electrophoresis techniques in an FDA-regulated biotechnology, pharmaceutical company is required.
  • Bachelor's degree in Chemistry, Biology, Molecular Biology, Biotechnology, Biochemistry, or related scientific discipline preferred.
  • Master's degree and 4+ years of relative experience preferred.

Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity

Salary Range: $110,800.00 - $150,800.00 annually
BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.
BeiGene logo

About BeiGene

Sourced by ZipRecruiter

BeiGene (NASDAQ: BGNE; HKEX: 06160; SSE: 688235) is a global, science-driven biotechnology company focused on developing innovative and affordable medicines to improve treatment outcomes and access for patients worldwide. With a broad portfolio of more than 40 clinical candidates, we are expediting development of our diverse pipeline of novel therapeutics through our own capabilities and collaborations. We are committed to radically improving access to medicines for two billion more people by 2030. BeiGene has a growing global team of over 8,200 colleagues across five continents. For more information, please visit www.beigene.com .

Industry

Health care and social assistance

Company size

5,001 - 10,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

2010

Social media

Twitter

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