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Quality Control Chemistry Jobs (NOW HIRING)

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 ...

QC Chemistry Technician

West Columbia, SC

$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 ...

Spectroscopic and wet chemistry testing will be performed independently. Participates in method qualifications and lab investigations. Responsibilities: * Independently execute QC chemistry testing ...

New

$25.50 - $34.50/hr

Perform GMP QC Chemistry methods including HPLC, UPLC, UV, and Particle Analysis via Dynamic Light Scattering * Execute HPLC (AEX) and NaOH plate reader-based assays to support process stat testing

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Quality Control Chemistry information

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How much do quality control chemistry jobs pay per hour?

As of Jun 8, 2026, the average hourly pay for quality control chemistry in the United States is $31.59, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $36.54 per hour, depending on experience, location, and employer.

What is the difference between Quality Control Chemistry vs Quality Assurance Specialist?

AspectQuality Control ChemistryQuality Assurance Specialist
CertificationsOften requires a Bachelor's in Chemistry or related field, with certifications like ASQ CQE or similarSimilar certifications, with focus on process audits and compliance
Work EnvironmentLaboratory settings, testing labs, manufacturing plantsOffice-based, audits, documentation, and process review environments
Primary FocusTesting raw materials, in-process, and finished products for quality and complianceDeveloping, implementing, and maintaining quality systems and procedures
Industry UsageCommonly used in manufacturing, pharmaceuticals, and chemical industriesUsed across similar industries but with a broader focus on quality systems

While both roles aim to ensure product quality, Quality Control Chemistry focuses on laboratory testing and analysis, whereas Quality Assurance Specialists develop and oversee quality systems and processes to prevent defects.

How much do QC chemists make in the US?

QC chemists in the US typically earn a median annual salary of around $55,000 to $70,000, depending on experience, education, and location. Entry-level positions may start lower, while experienced professionals with certifications can earn higher salaries, especially in regulated industries like pharmaceuticals and manufacturing.

What are some common challenges faced in a Quality Control Chemistry role, and how can they be addressed?

Quality Control Chemists often face challenges such as tight deadlines for product release, maintaining compliance with changing regulatory standards, and managing complex testing protocols. To address these, effective time management, continuous training on regulations, and strong attention to detail are essential. Additionally, collaborating with production and R&D teams helps resolve discrepancies quickly and ensures that quality standards are consistently met.

What is Quality Control Chemistry?

Quality Control Chemistry is a branch of chemistry focused on ensuring that products, especially in industries like pharmaceuticals, food, and manufacturing, meet quality and safety standards. Quality Control (QC) Chemists analyze raw materials, in-process samples, and finished products using a variety of analytical techniques to verify their composition and purity. Their work helps identify any deviations from regulatory or company standards, ensuring that products are safe and effective for consumers. QC Chemistry is crucial for compliance with government regulations and maintaining a company's reputation.

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

To thrive as a Quality Control Chemist, you need a solid understanding of analytical chemistry, laboratory techniques, and a bachelor's degree in chemistry or a related field. Familiarity with instruments such as HPLC, GC, FTIR, and LIMS, as well as knowledge of GMP/GLP regulations, is typically required. Attention to detail, critical thinking, and effective communication are valuable soft skills that enhance accuracy and teamwork. These competencies are crucial for ensuring product quality, regulatory compliance, and reliable laboratory operations.
More about Quality Control Chemistry jobs
What cities are hiring for Quality Control Chemistry jobs? Cities with the most Quality Control Chemistry job openings:
What are the most commonly searched types of Quality Control Chemistry jobs? The most popular types of Quality Control Chemistry jobs are:
What states have the most Quality Control Chemistry jobs? States with the most job openings for Quality Control Chemistry jobs include:
What job categories do people searching Quality Control Chemistry jobs look for? The top searched job categories for Quality Control Chemistry jobs are:
Infographic showing various Quality Control Chemistry job openings in the United States as of May 2026, with employment types broken down into 91% Full Time, and 9% Part Time. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $65,713 per year, or $31.6 per hour.
Manager, Quality Control Chemistry

Manager, Quality Control Chemistry

BeiGene, Inc.

Pennington, NJ • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 18 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

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