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Quality Assurance Research Jobs (NOW HIRING)

Collaborate with Quality Assurance, Research & Development, and Commercialization teams to address quality concerns and improve product consistency. * Identify opportunities to enhance production ...

Collaborate with Quality Assurance, Research & Development, and Commercialization teams to address quality concerns and improve product consistency. * Identify opportunities to enhance production ...

This person will assist in organization-wide quality activities under the direction of the Director of Quality Services within the Quality Assurance & Research Team. Location: Rahway, NJ 07065 ...

This person will assist in organization-wide quality activities under the direction of the Director of Quality Services within the Quality Assurance & Research Team. Location: Rahway, NJ 07065 ...

Work with QA, R&D, Director of Commercialization to discuss quality findings and develop solutions to enhance product consistency. · Continuous Improvement: Identify areas for improvement in ...

Work with QA, R&D, Director of Commercialization to discuss quality findings and develop solutions to enhance product consistency. · Continuous Improvement: Identify areas for improvement in ...

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Quality Assurance Research information

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$15

$44

$64

How much do quality assurance research jobs pay per hour?

As of Jul 19, 2026, the average hourly pay for quality assurance research in the United States is $44.87, according to ZipRecruiter salary data. Most workers in this role earn between $36.54 and $54.57 per hour, depending on experience, location, and employer.

What is quality assurance in research?

Quality assurance in research involves systematic processes to ensure that research methods, data collection, and analysis meet established standards for accuracy, reliability, and validity. For professionals in this field, it includes implementing protocols, conducting audits, and maintaining documentation to verify research integrity and compliance with industry guidelines.

What is the difference between Quality Assurance Research vs Quality Assurance Specialist?

AspectQuality Assurance ResearchQuality Assurance Specialist
Primary FocusDeveloping testing methods, analyzing data, improving quality processesImplementing quality standards, inspecting products, ensuring compliance
Required SkillsData analysis, research methodologies, testing proceduresInspection techniques, documentation, compliance knowledge
Work EnvironmentLaboratories, research facilities, development teamsManufacturing sites, production lines, quality control departments
CertificationsQuality assurance certifications, research methodology credentialsISO standards, Six Sigma, quality inspection certifications

While both roles focus on quality, Quality Assurance Research emphasizes developing testing methods and analyzing data to improve processes. In contrast, Quality Assurance Specialists focus on inspecting products and ensuring compliance during production. Understanding these differences helps in choosing the right career path or job role within the quality assurance field.

Is QA a difficult job?

Quality Assurance (QA) roles can be challenging as they require attention to detail, analytical skills, and knowledge of testing tools and processes. The difficulty level depends on the complexity of the projects and the experience of the individual, but it often involves problem-solving and thorough documentation.

What are some common challenges faced by professionals working in Quality Assurance Research, and how can they be addressed?

Professionals in Quality Assurance Research often encounter challenges such as keeping up with rapidly evolving industry standards, ensuring accurate data collection, and maintaining clear communication across interdisciplinary teams. Addressing these issues involves continuous learning, adopting robust documentation practices, and fostering collaboration through regular meetings with researchers, developers, and regulatory bodies. Staying organized and proactive in seeking feedback can also help mitigate potential errors and improve overall research quality.

Which pays more, QA or QC?

In the field of Quality Assurance Research, QA roles typically offer higher salaries than QC roles due to their focus on process improvement and prevention, often requiring more advanced skills and certifications. QC positions tend to be more inspection-focused and may have lower pay scales. Salary differences can vary based on industry, experience, and location.

What does a Quality Assurance Research professional do?

A Quality Assurance Research professional is responsible for ensuring that products, services, or processes meet established quality standards through systematic testing, analysis, and documentation. They design and implement tests, analyze data, identify issues or defects, and recommend improvements to enhance quality and compliance. Their work helps organizations maintain consistency, reliability, and regulatory compliance, ultimately improving customer satisfaction and reducing risks.

Are QA testers in demand in 2026?

Quality Assurance (QA) testers remain in demand as companies prioritize software quality and user experience. The role often requires familiarity with testing tools, scripting, and automation, with job growth driven by expanding technology sectors and increasing software complexity.

What are the key skills and qualifications needed to thrive as a Quality Assurance Research professional, and why are they important?

To excel in Quality Assurance Research, you need strong analytical skills, attention to detail, and typically a background in science, engineering, or a related field. Familiarity with quality management systems (such as ISO standards), statistical analysis tools, and laboratory information management systems (LIMS) is often required. Excellent problem-solving, communication, and teamwork abilities help you identify issues and collaborate effectively with cross-functional teams. These skills ensure consistent adherence to quality standards, accurate data reporting, and continuous improvement in research environments.
More about Quality Assurance Research jobs
What cities are hiring for Quality Assurance Research jobs? Cities with the most Quality Assurance Research job openings:
What states have the most Quality Assurance Research jobs? States with the most job openings for Quality Assurance Research jobs include:
Infographic showing various Quality Assurance Research job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 90% Full Time, 7% Part Time, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $93,338 per year, or $44.9 per hour.
QA R&D Chemist I

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago


Job description

Description

Tris Pharma, Inc. (www.trispharma.com) is a leading privately-owned U.S. biopharmaceutical company with a focus on development and commercialization of innovative medicines in ADHD, spectrum disorders, anxiety, pain and addiction addressing unmet patient needs. We have >150 US and International patents and market several branded ADHD products in the U.S. We also license our products in the US and ex-US markets. We have a robust pipeline of innovative products spanning neuroscience and other therapeutic categories employing our proprietary science and technology.


Our science and technology make us unique, but our team members set us apart; they are the engine fueling Tris' passion and innovation. Our colleagues understand the criticality of operating a successful business and take pride in the company's success. Equally importance to each team member is how we interact with one another on a daily basis. We believe in each other and in respectful, open and honest communications to help support individual and team success.


Located in Monmouth Junction, New Jersey, Tris has an immediate opening for a QA R&D Analytical Chemist, I


SUMMARY:

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 specifications to reflect changes in methods. Analytical support activities include, but are not limited to: method improvements, system equivalency, transfers, verifications, alternate source qualifications and authoring residual solvent, elemental impurity and nitrosamine risk assessments, as directed by R&D. The incumbent may also perform additional responsibilities including laboratory analyses of raw materials, in-process (IP) testing, finished products (FP), stability (ST) sample testing and analytical instrumentation maintenance and calibration.   


ESSENTIAL FUNCTIONS 

  • Carries out responsibilities in accordance with company policies, Standard Operating Procedures (SOPs) and state, federal and local laws 
  • Creates, reviews or revises SOPs, methods, specifications, verification protocols, reports and change control requests, as needed; Performs vendor qualification for raw materials and packaging materials
  • Performs testing of raw materials, packaging components, IP, FP and/or ST samples including dissolution, assay, related compounds analysis, content/blend uniformity, particle size distribution by Malvern/Sieve, bulk and Tap density, cleaning validation and other tests according to the analytical methods, United States Pharmacopeia (USP) procedures in a regulated laboratory environment 
  • Analyzes and interprets test results
  • Operates general analytical instruments during raw material, IP and FP testing such as High Pressure Liquid Chromatography (HPLC), UltraPerformance Liquid Chromatography (UPLC), Gas Chromatography (GC), Ultra Violet visible spectroscopy (UV/Vis), automatic titration, Infra-Red Spectroscopy (IR), Malvern Mastersizer, Thin Layer Chromatography (TLC) and dissolution apparatus (Distek)
  • Collaborates closely with R&D for analytical method transfer studies and other analytical method related issues
  • Assists with the identification and troubleshooting of problems with instrumentation and analytical preparations
  • Authors Residual Solvent, Elemental Impurity and Nitrosamine risk assessments
  • Meets project deadlines and performance standards, as assigned 
  • Maintains a clean and organized lab area
  • Complies with all Company policies and procedures, including safety rules and regulations
  • Adheres to GMPs and GDPs
  • Any other QA R&D related tasks assigned by Supervisor or QA R&D Management


Requirements

QUALIFICATIONS

Minimum education and years of relevant work experience


Bachelors degree in Chemistry or related science field and minimum 3 years lab experience in a cGMP related industry OR Masters degree in Chemistry or related science field and minimum 1 years lab experience in a cGMP related industry. 


Special knowledge or skills needed and/or licenses or certificates required:

  • Hands on experience with analytical instrumentation (i.e., UV, IR, HPLC, UPLC, Malvern Mastersizer, GC and/or dissolution instruments) in a pharmaceutical, biotechnology or academic setting
  • Proficiency with Microsoft Office
  • Verbal and written communication and skills
  • Ability to work independently and collaboratively, as required, in a fast paced, matrixed, team environment consisting of internal and external team members
  • Analytical thinking with problem-solving skills and the ability to adapt to changing priorities and deadlines 
  • Planning, organization and time management skills including the ability to support and prioritize multiple projects
  • Fluent in English (verbal and written)
  • Ability to identify and distinguish colors
  • Ability and willingness to work additional hours as required by business needs


Special knowledge or skills needed and/or licenses or certificates preferred:

  • Experience working with Food and Drug Administration (FDA), International Council on Harmonisation (ICH) guidelines, cGMPs and SOPs regulatory rules, regulations and guidelines
  • Proficiency with Empower software and other laboratory software
  • Experience with wet chemistry and chemistry related to sampling methods, quality control systems, analysis and documentation practices and procedures
  • Prior experience working in a QC lab  

Travel requirements

0%


Physical requirements

Laboratory based position

  •  Ability to use Personal Protective Equipment (PPE)
  •  Ability to stand for extended periods of time


Anticipated salary range: $85k - 95k. Base salary offered is contingent on assessment of candidate's education and experience level relative to requirements of the position and a review of related industry standards and internal equity.

Additional benefits: In addition to base salary, full-time employees are also eligible for incentives, including, but not limited to: bonus eligible, medical, dental, vision, Rx insurance, 401K with match, life insurance, paid Company Holidays, PTO, Paid Volunteer Time and Employee Resource Groups. 

Tris Pharma, Inc. offers a highly competitive compensation and benefits package. To build and enhance our diverse workforce, we encourage applications from individuals with disabilities, minorities, veterans, women, LGBTQ, etc. Tris Pharma, Inc. is an Equal Opportunity Employer. #LI-_