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Quality Control Analytical Scientist Jobs (NOW HIRING)

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 ...

Tris Pharma

QC Analytical Chemist

Monmouth Junction, NJ · On-site

$90K/yr

Our science and technology make us unique, but our team members set us apart; they are the engine ... Our Quality Control Department is growing and we have openings for QC Analytical Chemists at ...

Revance

Manager, Quality Control - Analytical

Newark, CA · Hybrid

$140K - $150K/yr

The Manager, Quality Control (QC) - Analytical is responsible for leading and overseeing the ... Master's of Science or Ph.D. in Chemistry, Biochemistry, Microbiology, Pharmaceutical Sciences, or ...

TeamSoft

Quality Control Analytical Color Matcher

Wharton, NJ · On-site

$25 - $33.50/hr

Quality Control Analytical Color Matcher Wharton, NJ 2nd Shift | 3:00 PM - 11:00 PM Pay Rate: 24 ... Associate's or Bachelor's degree in Chemistry, Biology, Cosmetic Science, or a related scientific ...

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

As of Jul 27, 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 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.

What are the key skills and qualifications needed to thrive as a Quality Control Analytical Scientist, and why are they important?

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 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.
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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 July 2026, with employment types broken down into 91% Full Time, 6% Part Time, and 3% Contract. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $71,807 per year, or $34.5 per hour.
Quality Control Analytical Scientist

Quality Control Analytical Scientist

Lynkx Staffing LLC

Saddle Brook, NJ

Full-time

Posted 22 days ago

Job description

Quality Control Analytical ScientistAllendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Devices industries in New Jersey. The QC Analytical Scientist will be a member of the Quality Control Department. As a Senior Member of the team the QC Analytical Scientist will be involved in various QC projects and should have a deep understanding of general QC flow and the Product Cycle.
  • Support internal and external customers to ensure that proper and timely execution of all aspects of the clinical analytical method life cycle across clients.
  • Support routine GMP testing as assigned. Mentor and train team members
  • Evaluate corporate and regulatory requirements along with coordination of activities for implementation of these requirements.
  • Write the contents of Analytical Method Transfer and Validation life cycle documentation including master plans, protocols, test methods, and reports.
  • Create validation project plan i.e., timelines and resources and provides status updates to management. Utilize statistical tools for evaluation of method validation and trending data.
  • Identify, evaluate, and implement continuous business process improvements.
  • Perform troubleshooting activities with respect to methods/assays, equipment malfunctions and investigations (Deviations and OOS).
  • Provide support during laboratory investigations.
  • Train QC personnel during method transfer and validation. Provide support during equipment qualification.
  • Consistently produce elevated level of documentation accuracy and clarity according to cGMP documentation practices.
  • Ability to set deadlines and prioritize work for self, group members, and support groups involved. Ability to review/approve work performed by coworkers for accuracy and alignment with procedures.
  • Indirectly may supervise cross functional teams including product development, QA, PMP, and Manufacturing.
REQUIREMENT
  • B.S Analytical Chemistry or other scientific field or MS/Ph.D. in Analytical Chemistry or other scientific field with demonstrated experience in Quality Control laboratories for biotechnology products.
  • 8-10 years of experience in the areas of method development, validation, and transfer.
  • Direct GMP Experience.
  • Proficiency in project management skills and tools.
  • Strong background and in-depth knowledge in analytical chemistry e.g. Flow Cytometry, ELISA, HPLC, CE, PCR, etc.
  • Extensive knowledge and experience of QC assay development, transfer and validation, along with cGMPs.
  • Strong Quality orientation with attention to detail required. Analytical and problem-solving skills required.
  • Excellent communication skills, both written and verbal, with all levels of the organization, including the ability to state opinions clearly, ask questions, seek clarification, communicate facts objectively, challenge when appropriate, and pursue issues to resolution.
  • Excellent presentation skills. Ability to communicate to upper management, across departments and within the immediate QC team.
  • Ability to create and manage work plans and timelines and independently manage competing priorities with limited instruction.
  • Highly motivated individual with good interpersonal skills that have proven effective in managing relationships and negotiating solutions while maintaining a level of approachability with colleagues both internal and external.
  • Must be familiar with GMP lab environment and Aseptic techniques.
Working EnvironmentMust have the ability to work in a team-oriented environment and with clientsMust be able to work during the weekend, holidays, or overtime and as required by the companyMay be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluidsMust utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, and liquid nitrogenMust have the ability to work with specialized equipmentMust be able to handle the standard/moderate noise of the manufacturing facilityMay work with hazardous materials and chemicals Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.