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Quality Control Analytical Scientist Jobs (NOW HIRING)

WuXi AppTec

QC Analytical Scientist

Middletown, DE · On-site

Reporting to the QC Analytical Lead, the QC Analytical Scientist will serve as a technical expert in analytical chemistry testing and laboratory operations in support of drug product manufacturing at ...

WuXi AppTec

QC Analytical Scientist

Middletown, DE · On-site

Reporting to the QC Analytical Lead, the QC Analytical Scientist will serve as a technical expert in analytical chemistry testing and laboratory operations in support of drug product manufacturing at ...

WuXi AppTec

QC Analytical Scientist

Middletown, DE · On-site

Overview Reporting to the QC Analytical Lead, the QC Analytical Scientist will serve as a technical expert in analytical chemistry testing and laboratory operations in support of drug product ...

Promega

Quality Control Analytical Scientist 3

Madison, WI · On-site

$90 - $120/hr

As QC Analytical Scientist 3 you will work primarily in the laboratory performing a wide diversity of tests required for API release and stability assessment. You will also be involved in new method ...

Replimune

Scientist I, Quality Control

Framingham, MA · On-site

$112K - $146K/yr

The Scientist I/II, QC Analytical will perform QC testing according to Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMP). This role may also include the ...

Regeneron Pharmaceuticals, Inc

NY · On-site

$92.20 - $150.60/hr

We are seeking a Principal Analytical Scientist to join our Quality Control team in Rensselaer, NY, supporting our IOPS organization on‑site. In this role, you will shape the future of QC ...

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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 Aug 19, 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 August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $71,807 per year, or $34.5 per hour.

QC Analytical Scientist

WuXi AppTec

Middletown, DE • On-site

Other

Posted 22 days ago

Job description

Reporting to the QC Analytical Lead, the QC Analytical Scientist will serve as a technical expert in analytical chemistry testing and laboratory operations in support of drug product manufacturing at WuXi STA’s Middletown, DE site. This role includes advanced execution and troubleshooting of analytical methods, stability studies, method transfers, and equipment qualification, as well as maintaining compliance with GMP, corporate quality standards, and global regulatory requirements. The QC Analytical Scientist will play a critical role in both startup and steady-state operations, ensuring timely and accurate testing for product release, validation, and regulatory inspections.

QC Analytical Testing and Support
  • Perform and review QC analytical testing for drug products, raw materials, packaging components, and stability samples in accordance with approved methods and SOPs.
  • Execute advanced analytical techniques including HPLC, UPLC, GC, dissolution, UV-Vis, TOC, Karl Fischer, and other relevant compendial and non-compendial methods.
  • Troubleshoot analytical instrumentation and methods, supporting investigations and continuous improvement.
  • Author, review, and revise test methods, SOPs, and technical documents.
  • Mentor and train QC Analysts and Associates in analytical techniques and best practices.
  • Other QC tasks assigned by analytical lead.
Regulatory Compliance and Documentation
  • Ensure all activities are conducted in strict compliance with cGMP, safety, and quality standards.
  • Maintain accurate, complete, and inspection-ready laboratory documentation.
  • Participate in method transfer, qualification, and validation of analytical methods and equipment.
  • Support client and regulatory audits by presenting data, explaining technical approaches, and preparing responses.
  • Escalate deviations, out-of-specification (OOS) results, or atypical findings promptly to the QC Analytical Manager.
  • Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related scientific discipline with 5+ years of QC analytical laboratory experience in a GMP-regulated pharmaceutical or biotechnology environment; OR
  • Master’s degree with 3+ years or PhD with 1+ years of relevant QC analytical laboratory experience.
  • Deep expertise in chromatographic and spectroscopic methods (HPLC/UPLC, GC, UV-Vis, TOC, KF, etc.) and data interpretation.
  • Demonstrated ability to lead laboratory investigations, troubleshoot instrumentation, and author technical reports.
  • Strong knowledge of GMP regulations, ICH guidelines, and data integrity principles (ALCOA+).

Preferred Qualifications

  • Experience in method transfer, qualification, and validation of analytical methods.
  • Familiarity with LIMS, Empower, or other electronic laboratory management systems.
  • Prior experience in a CDMO or multi-client environment.
  • Strong communication and collaboration skills to support cross-functional teams, audits, and regulatory inspections.

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 based on disability

This job description does not state or imply that the above are the only duties and responsibilities assigned to this position.  Employees holding this position will be required to perform any other job-related duties as requested by Management.

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