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Qc Chemist Jobs (NOW HIRING)

Position Summary The Quality Control Chemist is responsible for the review, approval, and maintenance of analytical chemistry documentation and quality records to ensure compliance with regulatory ...

Quality control chemist- 2nd shift Duration: 12 Months Location: Myerstown, PA 17067 Description: The Raw Material testing team is responsible for Quality Control testing of APIs and excipients used ...

Analytical Chemist (Quality Control) Location: Horsham, PA About the Opportunity Seeking Analytical Chemist to join a highly respected pharmaceutical contract development and manufacturing ...

Summary: QC Chemist personnel ensure that profitable, quality product is sold to the marketplace in compliance with the applicable ISO standards by the efficient, reproducible, and accurate analysis ...

QC Chemist

Holbrook, MA · On-site

$55K - $60K/yr

The QC Chemist is a laboratory bench position that performs routine release testing for raw materials, intermediates, and final products within a cGMP environment. PRINCIPAL DUTIES AND ...

QC Chemist/Lab Tech

Countryside, IL · On-site

$21 - $23/hr

Nyco Products - Lab Technician/QC Chemist At Nyco Products, the Lab Technician/QC Chemist is a very important position. Constantly on the move, you'll be responsible for assisting with research ...

Position Summary The Quality Control Chemist is responsible for the review, approval, and maintenance of analytical chemistry documentation and quality records to ensure compliance with regulatory ...

Quality Control Chemists must successfully complete the following training: Policy and Standard Operating Procedures, Laboratory orientation and safety training, training on specialized equipment and ...

QC Chemist

Baudette, MN · On-site

$48K - $52K/yr

Quality Control Chemists must successfully complete the following training: Policy and Standard Operating Procedures, Laboratory orientation and safety training, training on specialized equipment and ...

... quality control specifications Set up instruments and conduct sample tests; utilize a variety of ... Technical record-keeping techniques Bachelors of Science degree in chemistry or closely related ...

Sr QC Chemist

Boca Raton, FL · On-site

$90K - $110K/yr

Job Title: Sr QC Chemist Location: Boca Raton, FL Type: Direct Hire Compensation: $90,000-$110,000/year Work Model: Onsite - onsite Overview Pharmaceutical CDMO in Boca Raton, FL is seeking an ...

Sr QC Chemist

Boca Raton, FL · On-site

$90K - $110K/yr

Job Title: Sr QC Chemist Location: Boca Raton, FL Type: Direct Hire Compensation: $90,000-$110,000/year Work Model: Onsite - onsite Overview Pharmaceutical CDMO in Boca Raton, FL is seeking an ...

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Qc Chemist information

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How much do qc chemist jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for qc chemist 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 a QC chemist?

QC Chemists, or Quality Control Chemists, are professionals responsible for testing and analyzing the chemical composition of products to ensure they meet required standards and specifications. They work primarily in laboratories, using a variety of analytical instruments and techniques to assess product quality and safety. QC Chemists play a crucial role in industries such as pharmaceuticals, food and beverage, and manufacturing by identifying any deviations from quality standards and helping maintain regulatory compliance.

What are the key skills and qualifications needed to thrive as a QC chemist?

To thrive as a QC Chemist, you need a solid background in chemistry or a related science, attention to detail, and experience with quality control protocols, usually supported by a bachelor’s degree. Proficiency in laboratory instruments such as HPLC, GC, FTIR, and knowledge of LIMS or related data management systems is typically required. Strong analytical thinking, problem-solving abilities, and effective communication help QC Chemists excel in collaborative and regulated environments. These competencies ensure accurate testing, regulatory compliance, and the reliable release of safe, high-quality products.

What are some common challenges a QC chemist faces when ensuring product quality, and how are they typically addressed?

QC Chemists often encounter challenges such as detecting trace impurities, adhering to strict regulatory standards, and managing tight production deadlines. These are typically addressed by following rigorous standard operating procedures, utilizing advanced analytical instruments (like HPLC or GC), and collaborating closely with production and R&D teams. Continuous training and clear communication help minimize errors and ensure all quality benchmarks are consistently met.

What is the difference between Qc Chemist vs Quality Control Analyst?

AspectQc ChemistQuality Control Analyst
CredentialsBachelor's in Chemistry or related field, certifications often preferredBachelor's in Chemistry, Biochemistry, or related field, certifications optional
Work EnvironmentLaboratories, manufacturing plants, quality assurance departmentsLaboratories, quality control labs, manufacturing facilities
Employer & IndustryPharmaceutical, biotech, chemical manufacturing companiesPharmaceutical, food, cosmetics, chemical industries
Job FocusPerforming tests, analyzing data, ensuring product qualityConducting routine tests, recording results, maintaining quality standards

Both roles involve quality testing in laboratory settings within similar industries. A Qc Chemist often has a broader scope, including method development and data analysis, while a Quality Control Analyst primarily focuses on routine testing and documentation. Understanding these differences helps in choosing the right career path or job search focus.

How much do QC chemists make in the US?

QC chemists in the US typically earn an average salary of around $55,000 to $70,000 per year, depending on experience, location, and industry. Entry-level positions may start lower, while experienced professionals with certifications can earn higher salaries. Skills in laboratory techniques and familiarity with quality standards like GMP can influence compensation.

Is a QC chemist a good job?

A QC chemist is a valuable role in quality control, responsible for testing and analyzing raw materials and finished products to ensure compliance with standards. The job typically requires attention to detail, knowledge of laboratory techniques, and sometimes certifications like a degree in chemistry or related fields. It offers stable employment opportunities in industries such as pharmaceuticals, manufacturing, and food production.
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Infographic showing various Qc Chemist job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 87% Full Time, 7% Part Time, 3% Contract, and 1% Nights. Highlights an 92% Physical, 4% Hybrid, and 4% Remote job distribution, with an average salary of $65,713 per year, or $31.6 per hour.

Quality Control Chemist

Houston, TX

Full-time

Re-posted 9 days ago


Job description

Position Summary

The Quality Control Chemist is responsible for the review, approval, and maintenance of analytical chemistry documentation and quality records to ensure compliance with regulatory and accreditation requirements. This role supports Eagle Analytical’s Quality Management System by reviewing analytical methods, validation documentation, laboratory data, reports, and quality investigations while ensuring adherence to cGMP, cGLP, ISO 17025, A2LA, and USP standards. The position works closely with laboratory operations to maintain data integrity, regulatory compliance, and continuous improvement across chemistry testing functions.

What You Will Do

  • Ensure compliance with Eagle Analytical policies, Standard Operating Procedures (SOPs), and the Quality Management System.
  • Interpret and apply regulatory and accreditation standards, including ISO 17025, cGMP, cGLP, USP, and A2LA requirements.
  • Support regulatory inspections, client audits, and accreditation assessments as required.
  • Write, review, and approve SOPs, work instructions, forms, and quality records to ensure regulatory compliance and operational consistency.
  • Review and approve analytical test methods and related documentation for chemistry testing, including UV-Vis spectrophotometry, HPLC, HPLC-MS/MS, GC-MS, and other analytical instrumentation.
  • Review laboratory test reports, chemistry logs, worksheets, validation protocols, and validation reports.
  • Ensure analytical data integrity, accuracy, completeness, and traceability.
  • Review and approve quality investigations, including Out-of-Specification (OOS), Nonconformance Reports (NCR), Deviations (DV), Corrective and Preventive Actions (CAPA), change controls, and customer complaints.
  • Evaluate root cause analyses and corrective action plans for process and laboratory-related issues.
  • Create audit finding reports and determine appropriate corrective and preventive actions.
  • Support and conduct internal audits of quality systems and documentation.
  • Perform routine walk-through audits to ensure ongoing compliance across laboratory departments.
  • Manage auditing, storage, and retention of quality documentation and quarantined materials.
  • Prepare and maintain quality-related training materials as assigned.
  • Support continuous improvement initiatives related to quality systems, documentation, and laboratory compliance.
  • Assist in creating and maintaining quality manuals, procedures, and other controlled quality documents.
  • Perform additional duties and special projects as assigned to support quality and regulatory objectives.

Who You Are

  • Bachelor’s degree in Chemistry, Analytical Chemistry, or a related scientific discipline required.
  • Experience in a regulated laboratory environment (ISO 17025, cGMP, cGLP) preferred.
  • Experience supporting analytical chemistry testing laboratories is strongly preferred.
  • Strong understanding of analytical chemistry techniques and instrumentation, including HPLC, HPLC-MS/MS, GC-MS, and UV-Vis.
  • Working knowledge of method validation, data review, and laboratory quality systems.
  • Experience reviewing GMP/GLP documentation and quality investigations.
  • Strong attention to detail and commitment to data integrity and compliance.
  • Excellent written and verbal communication skills.
  • Ability to work independently while collaborating effectively with cross-functional teams.
  • Proficiency with Microsoft Office applications and electronic document management systems.
  • ASQ preferred

Who We Are

Serving customers since 2004, Eagle offers the highest quality in preparation testing for sterility, bacterial endotoxins, microbial detection, beyond-use dating (BUD) determination and active ingredient potency. State-of-the-art equipment, combined with the experience and knowledge of our team, makes Eagle the best choice for all testing needs. The Eagle team is committed not only to performing the best quality control testing, but also working relentlessly with our customers on solutions if tests receive unexpected results. Learn more at www.eagleanalytical.com.Â