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Stability Data Reviewer Jobs (NOW HIRING)

FAR Inspections

Vacancy Data Reviewer

Salt Lake City, UT · On-site

$25 - $35/hr

FAR Inspections is a leading provider of property data for mortgage lenders nationwide ... Based in Reno, NV, we have a 12-year track record of excellence and stability in the mortgage field ...

Herbalife

Manager, Stability

Torrance, CA · Hybrid

HOW YOU'LL MAKE AN IMPACT: • Lead and oversee stability studies, including protocol execution, sample management, data review, statistical analysis, trending, and reporting. • Serve as a primary ...

Herbalife

Manager, Stability

Torrance, CA · Hybrid

Lead and oversee stability studies, including protocol execution, sample management, data review, statistical analysis, trending, and reporting. Serve as a primary communication lead for stability ...

Herbalife

Manager, Stability

Torrance, CA · On-site

HOW YOU'LL MAKE AN IMPACT: • Lead and oversee stability studies, including protocol execution, sample management, data review, statistical analysis, trending, and reporting. • Serve as a primary ...

Avecia Pharma

Quality Data Reviewer, 2nd Shift

Milford, MA · On-site

$100 - $125/hr

Review quality data and reports (including stability and release) for compliance against specifications, GMP regulations, and scientific technique. * Author's stability reports, COAs, data summaries ...

New

Nitto Denko

Quality Data Reviewer, 2nd Shift

Milford, MA · On-site

$91K - $111K/yr

Review quality data and reports (including stability and release) for compliance against specifications, GMP regulations, and scientific technique. * Author's stability reports, COAs, data summaries ...

New

Nitto Denko Corp.

$91K - $111K/yr

Review quality data and reports (including stability and release) for compliance against specifications, GMP regulations, and scientific technique. * Author's stability reports, COAs, data summaries ...

Vaxcyte

Stability Manager

San Carlos, CA · On-site

$147K - $171K/yr

Produce impactful PowerPoint presentations to effectively communicate stability data to diverse ... Authors, reviews, revises, and approves SOP's, stability protocols and reports, memo's, regulatory ...

Eurofins

QC Data Reviewer - LNP and Lipids

Boston, MA · On-site

Review analytical data packages from stability studies, method development, and investigations for LNP and lipid-based products. * Evaluate OOS/OOT investigation reports for completeness, scientific ...

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Stability Data Reviewer information

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How much do stability data reviewer jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for stability data reviewer in the United States is $26.24, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $36.30 per hour, depending on experience, location, and employer.

What is a stability data reviewer?

Stability Data Reviewers are professionals responsible for analyzing and evaluating stability data generated during the pharmaceutical development process. Their main role is to ensure that medicines and other products maintain their intended quality, safety, and efficacy throughout their shelf life. They review data from stability studies, check for compliance with regulatory guidelines, and prepare reports for regulatory submissions. Their expertise helps ensure that products meet all required standards before reaching the market.

What skills and qualifications are needed to be a stability data reviewer?

To thrive as a Stability Data Reviewer, you need a strong background in pharmaceutical sciences, chemistry, or related fields, often supported by a relevant degree and experience with stability studies. Familiarity with regulatory guidelines (such as ICH), Laboratory Information Management Systems (LIMS), and data analysis software is typically required. Attention to detail, critical thinking, and effective communication are essential soft skills in this role. These competencies ensure accurate review and interpretation of stability data, supporting regulatory compliance and product quality in the pharmaceutical industry.

What challenges do stability data reviewers face when ensuring data integrity and compliance?

Stability Data Reviewers often encounter challenges such as managing large volumes of complex data, keeping up with evolving regulatory requirements, and ensuring consistent documentation across multiple studies. Attention to detail is critical, as even minor discrepancies can impact product quality assessments and regulatory submissions. Collaboration with laboratory analysts, quality assurance staff, and regulatory teams is essential to address data gaps, clarify findings, and maintain compliance throughout the review process.

What cities are hiring for Stability Data Reviewer jobs?

Cities with the most Stability Data Reviewer job openings:

What states have the most Stability Data Reviewer jobs?

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Infographic showing various Stability Data Reviewer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, and 3% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $54,583 per year, or $26.2 per hour.

Stability Data Specialist

Lexington, MA • On-site

Eurofins USA PSS Insourcing Solutions
See more jobs at Eurofins USA PSS Insourcing Solutionsexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Company Description

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

If you’re looking for a rewarding career, a place to call home, apply with us today!

Job Description

This is a hybrid, non-laboratory role supporting Quality and Analytical functions. The successful candidate will collaborate with internal teams and external partners to ensure data integrity, regulatory compliance, and timely execution of deliverables.

Key Responsibilities

  • Collaborate with departmental colleagues to complete assignments under supervision.
  • Review and interpret analytical data with client support; contribute to technical reports and regulatory documentation.
  • Evaluate QC testing data for small molecule and/or biologics methods from external vendor laboratories.
  • Enter GMP data into validated database systems accurately and efficiently.
  • Verify data and trending tables for inclusion in regulatory submissions.
  • Build and manage stability studies within validated systems, as applicable.
  • Ensure GMP data aligns with current specifications; generate Certificates of Analysis (COAs) when required.
  • Monitor and trend reference standards and analytical data.
  • Identify and escalate routine technical issues or vendor-related concerns.
  • Troubleshoot basic issues using available resources and guidance.
  • Travel between Lexington and Cambridge client sites as needed.
Qualifications
  • Bachelor’s degree in Chemistry, Biology, or a related field.
  • Minimum of 2 years of relevant industry experience.
  • Prior experience in Quality Control, Quality Assurance, or a GMP-regulated environment is required.
  • Experience in Analytical Development is preferred.
  • Familiarity with analytical methods for biologics or small molecule products is a plus.
  • Solid understanding of GMP principles and regulatory compliance.
  • Strong communication skills; able to document and report issues clearly and promptly.
  • Effective time management and multitasking abilities in a cross-functional team setting.
  • Must be authorized to work in the U.S. permanently without restriction or sponsorship

Additional Information

Position is Full Time, Monday-Friday, 8am-5pm. Candidates currently living within a commutable distance of Lexington, MA are encouraged to apply. Occasional travel (approximately 1–2%) to the Cambridge, MA site may be required.

Excellent full-time benefits include:

  • Comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
  • Eligibility for yearly goal-based bonus & merit-based increases
  • Compensation: $31.00-$35.00 per hour based on education and related experience

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.