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Quality Control Analytical Scientist Jobs (NOW HIRING)

Astrix Inc

Analytical Scientist

Thousand Oaks, CA · On-site

$57 - $62/hr

Pay Rate Low: 57.00 | Pay Rate High: 62.00 6 month contract Pay: $57-62/hr Summary As a QC Analytical Scientist II, you will support various Quality Control activities within the AQC department. Key ...

WuXi AppTec

QC Raw Material Scientist

Middletown, DE · On-site

Reporting to the QC Analytical Lead, the QC Raw Material Scientist will serve as a technical expert in analytical chemistry testing and laboratory operations supporting the release of raw materials ...

WuXi AppTec

QC Raw Material Scientist

Middletown, DE · On-site

Reporting to the QC Analytical Lead, the QC Raw Material Scientist will serve as a technical expert in analytical chemistry testing and laboratory operations supporting the release of raw materials ...

WuXi AppTec Group

NY · On-site

Overview Reporting to the QC Analytical Lead, the QC Raw Material Scientist will serve as a technical expert in analytical chemistry testing and laboratory operations supporting the release of raw ...

WuXi AppTec

QC Raw Material Scientist

Middletown, DE · On-site

Overview Reporting to the QC Analytical Lead, the QC Raw Material Scientist will serve as a technical expert in analytical chemistry testing and laboratory operations supporting the release of raw ...

Actalent

QC Analytical Chemist

Verona, WI · On-site

$22 - $25/hr

QC Analytical Chemist Shift: 2nd shift 11:30am - 8:00pm Mon - Thurs & 9:30am - 6:00pm Friday We are ... This is an excellent opportunity for recent graduates or early-career scientists looking to gain ...

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Quality Control Analytical Scientist information

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How much do quality control analytical scientist jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for quality control analytical scientist in the United States is $34.52, according to ZipRecruiter salary data. Most workers in this role earn between $24.76 and $39.66 per hour, depending on experience, location, and employer.

What does a quality control analytical scientist do?

A Quality Control Analytical Scientist is responsible for testing and analyzing materials, products, and processes to ensure they meet established quality standards and regulatory requirements. They use a variety of laboratory instruments and techniques, such as chromatography and spectroscopy, to evaluate chemical, physical, and biological properties. Their work helps ensure the safety, efficacy, and consistency of products in industries like pharmaceuticals, biotechnology, and manufacturing. Additionally, they document results, troubleshoot issues, and collaborate with other teams to maintain quality throughout the production process.

What are the key skills and qualifications needed to thrive as a quality control analytical scientist?

To thrive as a Quality Control Analytical Scientist, you need a solid background in chemistry, analytical techniques, and a relevant degree such as a BS or MS in chemistry, biochemistry, or a related field. Proficiency in laboratory instrumentation like HPLC, GC, and spectrophotometry, along with knowledge of GMP/GLP regulations and possible certifications, is typically required. Attention to detail, problem-solving, and effective communication are essential soft skills for accurate data interpretation and teamwork. These skills ensure precise analytical results, regulatory compliance, and the integrity of product quality in regulated industries.

What are some typical challenges faced by quality control analytical scientists when working with new pharmaceutical products?

Quality Control Analytical Scientists often encounter challenges when validating analytical methods for new pharmaceutical products, such as ensuring accuracy, reproducibility, and compliance with strict regulatory standards. They may need to troubleshoot unexpected results, adapt to evolving testing technologies, and coordinate closely with cross-functional teams like R&D and manufacturing to resolve issues swiftly. Attention to detail and strong communication skills are essential in addressing these challenges and ensuring product quality throughout the development and production lifecycle.

What is the difference between Quality Control Analytical Scientist vs Quality Control Chemist?

AspectQuality Control Analytical ScientistQuality Control Chemist
CredentialsBachelor's or Master's in Chemistry, Biochemistry, or related field; relevant certificationsBachelor's degree in Chemistry or related field; certifications are common but not always required
Work EnvironmentLaboratories within pharmaceutical, biotech, or manufacturing companiesLaboratories in similar industries, often performing routine testing
Job FocusDeveloping and validating analytical methods, data analysis, ensuring compliancePerforming routine sample testing, preparing reports, and maintaining documentation

The main difference is that the Quality Control Analytical Scientist typically focuses on method development, validation, and data analysis, while the Quality Control Chemist primarily conducts routine testing and sample analysis. Both roles are essential in quality assurance within manufacturing industries, but the Analytical Scientist often requires a deeper understanding of analytical techniques and method validation processes.

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Quality Control Analytical Scientist jobs near you
Infographic showing various Quality Control Analytical Scientist job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $71,807 per year, or $34.5 per hour.

Manager, Quality Control & Analytical Development

Vacaville, CA • On-site

Oath
Non-Profits • 1 - 10 employees
Learn more about Oathexternal

$100K - $130K/yr

Full-time

Posted 15 days ago

Job description

About Oath
Oath is a leading microbial sciences company that utilizes natural soil biology to offer innovative solutions to some of the most critical challenges facing our planet - the climate crisis and the shift to sustainable agriculture. We imagine a world where these crises are not just alleviated, but reversed, replenishing Earth's microbiomes.
Our solution has moved beyond the lab and into real-world deployment, focused on improving farmer livelihoods with teams in Rwanda, Europe, the United States, and expanding. When you join Oath, you become part of a collaborative network that prioritizes high quality scientific work. You will be working alongside trained scientists, talented commercial teams, and a broad network of partners-an ecosystem designed to help you do your best work and grow your capabilities.
Position Summary
We are seeking an experienced Manager, Quality Control & Analytical Development to lead QC and analytical assay development for Oath's live microbial products. This role will own QC methods, specifications, and production batch review and release, while developing and validating fit-for-purpose assays to support manufacturing and product quality. You will ensure microbial products meet quality requirements throughout cultivation, fermentation, downstream processing, formulation, and storage, and translate analytical methods into robust, scalable QC tools for internal and external manufacturing.
Key Responsibilities
Quality Control & Batch Release
  • Own QC review and release of production batches against established specifications.
  • Define and maintain product specifications, release criteria, sampling plans, and QC testing requirements.
  • Review QC data, batch records, COAs/COCs, and supporting documentation.
  • Lead investigations of deviations, out-of-specification results, and product quality issues.
  • Establish stability and shelf-life testing and monitor product quality trends.
Analytical Assay Development & Validation
  • Develop, optimize, and validate quantitative assays supporting manufacturing, QC, and product release.
  • Establish robust methods for microbial titer, viability, sporulation, purity, stability, and other key quality attributes.
  • Apply techniques including CFU methods, qPCR/qRT-PCR, flow cytometry, sequencing, and other relevant analytical methods.
  • Ensure assays are reproducible, scalable, and fit for manufacturing routine QC use.
Manufacturing & Method Transfer
  • Lead transfer and implementation of QC methods at CROs and CMOs/CDMOs.
  • Define testing requirements and ensure consistent execution of Oath methods and specifications.
  • Review external QC data, batch documentation, and technical reports.
  • Partner with manufacturing teams to troubleshoot quality issues and improve QC processes.
Quality Systems & Documentation
  • Develop and maintain QC SOPs, analytical methods, specifications, protocols, and reports.
  • Establish appropriate sample tracking, data management, and QC documentation practices.
Cross-Functional Collaboration
  • Partner closely with Production, Bioprocess Development, R&D, Regulatory, Supply Chain, and Field Science.
  • Provide data-driven recommendations on product quality, manufacturing, formulation, and stability.
  • As the team grows, mentor and manage scientists and research associates.
Qualifications
Required
  • PhD or MS in Microbiology, Biotechnology, Analytical Sciences, Fermentation Science, or a related field, with relevant industry experience.
  • Experience with QC testing, product specifications, method validation, and production batch review/release.
  • Experience developing and validating quantitative assays for microbial, biological, or fermentation-based products.
  • Experience working with manufacturing teams, CROs, CMOs/CDMOs, or external testing laboratories.
  • Strong ownership, communication, documentation, and cross-functional leadership skills.
Preferred
  • Experience in agriculture, agricultural biotechnology, biologicals, or microbial products strongly preferred.
  • Experience with deviations, OOS investigations, stability programs, and quality systems preferred.

Job Type: Full-time, non-exempt position in the United States. At this time, Oath, Inc. is not able to provide visa sponsorship or work authorization support.
Location: Vacaville, CA, 3 days a week with international travel to Europe up to 20%
Compensation: $100,000 - $130,000

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