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Quality Control Chemistry Jobs (NOW HIRING)

Quality Control (QC) Chemist - Inhalation Products (MDI Focus) Location: Fall River, MA (On-site ... Bachelor's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or Physics (highly ...

Quality Control (QC) Chemist

Fall River, MA ยท On-site

$65K - $105K/yr

Quality Control (QC) Chemist - Inhalation Products (MDI Focus) Location: Fall River, MA (On-site ... Bachelor's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or Physics (highly ...

QC Chemist

Central Islip, NY ยท On-site

$65K - $90K/wk

Bachelor's degree in Chemistry or a related scientific field. * 2-15 years of experience in a QC/analytical chemistry role within the pharmaceutical sector. * Strong understanding of lab testing and ...

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Quality Control Chemist

Ottawa, IL ยท On-site

$50K - $80K/yr

Bachelor's degree in Chemistry or closely related scientific discipline. * 1-3 years of quality control experience in personal care, cosmetics, OTC pharmaceuticals, or related manufacturing ...

QC Chemistry Technician, 3rd Shift

Fishers, IN ยท On-site

$18.50 - $23.50/hr

Performs sample management activities for Quality Control Chemistry Laboratory including management of samples from clean utilities, components, raw materials, in-process samples, finished product ...

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Quality Control Chemistry information

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How much do quality control chemistry jobs pay per hour?

As of Jul 6, 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.

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:
Infographic showing various Quality Control Chemistry job openings in the United States as of June 2026, with employment types broken down into 17% As Needed, 49% Full Time, 17% Part Time, and 17% Temporary. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $65,713 per year, or $31.6 per hour.

Quality Control Chemistry Sample Management Coordinator

InjectEZ LLC

West Columbia, SC

Other

Posted 17 days ago


Job description

Description

QC Chemistry Sample Management Coordinators are to manage the receipt, storage, organization, and disposal of Analytical Services laboratory samples in a high-growth, fast-paced, dynamic work environment while ensuring compliance with FDA and DEA regulations. The qualified individual will be responsible for receiving and logging samples into the company's Laboratory Information Management System (LIMS) while ensuring compliance of QC practices. The qualified individual will assist in maintaining a flexible organization to allow fast changing manufacturing priorities to occur with minimum disruption and avoid backlogs. The individual will assist with additional work duties or responsibilities as evident or required.

Essential Duties and Responsibilities:

  • Receive and log samples in accordance with SOPs and GMP requirements through LIMS or other tracking systems.
  • Distributes, bags, and labels samples according to required testing needs ensuring sample management.
  • Maintains organization in sample receiving.
  • Identifies samples needed for outside testing and follows procedures for shipping to third party labs.
  • Maintains an organized and clean sample storage area for all active and tested samples.
  • Communicates with appropriate persons concerning ID and lot number discrepancies.
  • Completes waste destruction forms and submits/files them accordingly.
  • Oversee and supervise sample waste disposal within the laboratory.
  • Recognize and initiate any continuous improvement opportunities in sample handling, documentation, or communication processes to improve efficiency, accuracy, and compliance throughout the sample lifecycle.ย 

Supplemental Functions:

Assist with the overall cleanliness of the QC laboratory to ensure compliance with all cGMP requirements.

Provide guidance to management to resolve all QC compliance-related observations, issues, problems, discrepancies, and violations of company policies/procedures.

Performs other similar duties as assigned or apparentย 

Requirements

Job Specifications and Qualifications:

  • Experience using LabVantage or similar software preferred.
  • Ability to use a computer and different programs efficiently.

Knowledge & Skills:ย 

  • Must be detailed oriented and have excellent organizational skills.
  • Must possess effective written and oral communication skills and be able to handle multiple tasks within limited timeframes.
  • Knowledge of FDA manufacturing/regulatory quality systems regulations, qualification, facilities and investigation requirements.
  • Ability and willingness to change direction and focus to meet shifting organizational and sample demands.
  • Ability to create and contribute to an environment that values people, encourages trust, teamwork, and open communication, and provides participation, learning, feedback and recognition.
  • Ability to effectively manage oneself, demonstrates integrity, be productive under pressure, and achieve development goals.ย 
  • Ability to effectively manage a multitude of resources and to be accurate and current with data and information.
  • Well-developed knowledge of the consumer/customer demonstrated through continuous efforts to exceed their expectations.
  • Broad perspective that aligns decisions to organizational objectives and ย ย ย ย ย long-term consequences of day-to-day activities.
  • Ability to take strategic objectives and accept accountability, motivate, and ย ย ย ย ย influence others, thinks globally and leverages diversity.

Education/Experience:

  • Bachelor's degree in Science or related field required (Chemistry, Microbiology or Biology).
  • Experience with cGMP documentation systems and with implementation of QC systems.
  • Specific expertise, skills and knowledge within laboratory compliance gained through education and experience.
  • Salary range: Based on experience. ย 

Working Conditions / Physical Requirements:

  • Position requires bending, typing, climbing, lifting, reaching, vision, standing, sitting, walking, and hearing.
  • Position encounters the following environmental factors: hazardous materials including HPLC solvents, chemical reagents, acids and other non-specified hazardous materials that are project specific.
  • Position requires lab coats, safety glasses, respiratory and other non-specified protective equipment to be worn as necessary.