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Qa Chemist Jobs (NOW HIRING)

Qa/qc Specialist

Bridgeton, MO · Hybrid

$28 - $45/hr

Perform comprehensive QA review of laboratory testing data and documentation, focusing on analytical chemistry methods including HPLC, GC, UV-Vis, and dissolution. * Verify mathematical calculations ...

Analytical QA Supervisor Location: Fall River, MA Experience Required: 5 - 15 Years Job Type ... The ideal candidate will bring a strong analytical chemistry background, especially within a ...

The Quality Assurance (QA) Research and Development (R&D) Chemist I supports Quality Control (QC) and Analytical R&D (AR&D) activities by initiating appropriate change controls and updating ...

The Quality Assurance (QA) Research and Development (R&D) Chemist I supports Quality Control (QC) and Analytical R&D (AR&D) activities by initiating appropriate change controls and updating ...

S. in Chemistry required, M.S. in Chemistry a plus * Minimum 5+ years of Quality Assurance experience in chemical manufacturing, pharmaceutical manufacturing, food manufacturing, or a related ...

Bachelor's degree in Chemistry, Biology, or related scientific discipline with 3-5 years of applicable Quality Assurance environment preferable in the pharmaceutical OTC industry. * Master's degree ...

Plant QA Manager REPORTS TO: Vice President of Quality Assurance INDIRECTLY REPORTS TO: Plant ... chemistry related testing related to product requirements (color, Brix, pH, yeast, mold, APC) • ...

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Qa Chemist information

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How much do qa chemist jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for qa chemist in the United States is $30.99, according to ZipRecruiter salary data. Most workers in this role earn between $24.04 and $35.58 per hour, depending on experience, location, and employer.

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

AspectQa ChemistQuality Control Analyst
Required CredentialsBachelor's in Chemistry or related field, certifications like CQE often preferredBachelor's in Chemistry, Biology, or related field, similar certifications
Work EnvironmentLaboratories, manufacturing plants, quality assurance departmentsLaboratories, manufacturing facilities, quality testing labs
Employer & Industry UsagePharmaceutical, food, cosmetics, chemical industriesPharmaceutical, food, beverage, cosmetics industries
Common Search & ComparisonYesYes

Qa Chemists and Quality Control Analysts often share similar educational backgrounds and work environments within manufacturing and quality assurance sectors. While Qa Chemists may focus more on developing and validating quality processes, Quality Control Analysts primarily perform testing and inspection of products. Both roles are essential for ensuring product safety and compliance, and their responsibilities often overlap in industry settings.

How does a QA chemist typically interact with production and R&D teams in a manufacturing environment?

QA Chemists play a key role in ensuring product quality by regularly collaborating with both production and R&D teams. They review raw material specifications, conduct analytical testing, and provide feedback on batch releases to production staff. When new formulations or processes are introduced by R&D, QA Chemists validate methods and help troubleshoot any quality issues that arise during scaling. This cross-functional collaboration is essential for maintaining compliance with regulatory standards and continuous process improvement.

What is a QA chemist?

QA Chemists, or Quality Assurance Chemists, are professionals responsible for ensuring that chemical products meet required safety and quality standards. They conduct laboratory tests, analyze samples, and review production processes to detect and prevent defects or contamination. QA Chemists also document findings, maintain compliance with regulatory guidelines, and help improve quality control protocols. Their work is crucial in industries such as pharmaceuticals, food and beverage, and manufacturing to ensure product safety and consistency.

What are the key skills and qualifications needed to thrive as a QA chemist, and why are they important?

To thrive as a QA Chemist, you need a solid background in chemistry, laboratory techniques, and quality assurance principles, often backed by a bachelor's degree in chemistry or a related field. Familiarity with analytical instruments like HPLC, GC, and spectrophotometers, as well as knowledge of GMP regulations and LIMS software, is typically expected. Strong attention to detail, problem-solving abilities, and effective communication skills set top performers apart in this role. These skills and qualities are vital for ensuring product quality, regulatory compliance, and maintaining the integrity of laboratory results.
More about Qa Chemist jobs
What cities are hiring for Qa Chemist jobs? Cities with the most Qa Chemist job openings:
What states have the most Qa Chemist jobs? States with the most job openings for Qa Chemist jobs include:
Infographic showing various Qa 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, 3% Part Time, 7% Contract, and 1% Nights. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $64,466 per year, or $31 per hour.

Quality Assurance Specialist

Cosmetic Solutions

Boca Raton, FL

Full-time

Posted 15 days ago


Job description

Who we are:

 

Cosmetic Solutions is a leader in the development and manufacturing of scientifically proven, innovative personal care products. With a focus on, face, body, hair, OTC, and professional use formulations, we create some of the most cost effective, high quality and powerful products on the market. 

Providing world class services to up and coming businesses, large established brands, physicians, estheticians and other skin care professionals; we specialize in research & development, custom formulation, graphic design, manufacturing, packaging and delivery. 

 

Job Title: Quality Assurance Specialist

Organizational Relationships

Reports to:

  • QA Manager

Supports:

  • QA/QC, Operations, Sales

 

Responsibilities will include, but are not limited to:

 

1. Good Manufacturing Practices (GMP):

  •  Ensure Compliance with GMP regulations throughout the manufacturing process.
  • Conduct regular audits and inspections to verify adherence to GMP standards.
  • Develop and implement strategies to continuously improve GMP compliance.

2. Quality Systems Management:

  • Maintain and improve the company’s quality management system (QMS).
  • Identify areas for process improvement and implement effective quality control measures.
  • Collaborate with cross-functional teams to ensure alignment with quality objectives.

3. Corrective and Preventative Actions (CAPAs):

  • Lead investigations into quality issues and non-conformances.
  • Develop CAPA plans to address root causes and prevent recurrence of quality issues.
  • Monitor and track the implementation of CAPAs to ensure effectiveness.

4. Deviations Management:

  • Investigate deviations from established procedures and specifications.
  • Develop and implement corrective actions to address deviations and prevent recurrence.

5. Document Control:

  • Ensure the accuracy, completeness, and integrity of quality-related documentation.
  • Manage document change control processes and maintain document repositories.
  • Lead root cause investigations for quality issues and customer complaints, implementing corrective and preventive actions.
  • Work cross-functionally with sales, manufacturing and supply chain teams to address quality concerns that could affect customer satisfaction or regulatory compliance.
  • Enter scanned work orders into the tracking system.
  • Review batch cards and log into tracker.
  • Review finished goods work orders and update tracker.
  • Send finished goods (FG) samples to the laboratory.
  • Print and review finished goods work orders.
  • Attach green status stickers to bulk material.
  • Review and approve labels for work orders.
  • Verify that all work orders include the required SDS documentation.
  • Review the production schedule for accuracy and updates.

6. Standard Operating Procedures (SOPs):

  • Develop, review, and update SOPs to reflect current best practices and regulatory requirements.
  • Ensure SOPs are followed consistently throughout the organization.
  • Provide training and support to employees on SOPs and quality processes.

7. Subject Matter Expertise & Program Ownership (Progressive Responsibility):

  • Over time, the Quality Assurance Specialist will develop into a Subject Matter Expert (SME) and assume ownership of key Quality Systems programs in alignment with 21 CFR Parts 210/211. Core areas include Annual Product Reviews (APR/PQR), Supplier Qualification, eQMS administration and internal audit/inspection readiness. The role is expected to drive continuous improvement through quality metrics trending, training support, and ensuring sustained GMP compliance across operations.

Experience:

  • Previous experience working in a manufacturing environment, preferably in a regulated industry (e.g., pharmaceuticals, medical devices, food).
  • Strong understanding of Good Manufacturing Practices (GMP) and regulatory requirements (e.g., FDA, ISO).
  • Experience with quality systems management, CAPAs, deviations, document control, and SOPs.
  • Excellent analytical and problem-solving skills.
  • Effective communication and collaboration abilities. Must be able to read, write, and speak in English.
  • Detail-oriented with a commitment to quality and compliance.

Education:

 

  • Bachelors degree in a related field preferred (e.g., Quality Assurance, Chemistry, Biology, Engineering).

 

Equal Employment Opportunity

Cosmetic Solutions is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.