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Stability Data Reviewer Jobs (NOW HIRING)

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 ...

Rentschler

Quality Control Data Reviewer

Milford, MA · On-site

$90K - $110K/yr

Data review may consist of all/some of the following: • Review and approval of QC test analytics; in process, release, stability, validation • Track, organize, prepare QC test results for product ...

Rentschler

Quality Control Data Reviewer

Milford, MA · On-site

$90K - $110K/yr

Data review may consist of all/some of the following: • Review and approval of QC test analytics; in process, release, stability, validation • Track, organize, prepare QC test results for product ...

Vaxcyte

Stability Manager

San Carlos, CA · On-site

$134K - $162K/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 ...

Moderna, Inc.

Director, CMC Stability

Norwood, MA · On-site

In partnership with Quantitative Sciences, oversee stability data trending, statistical analysis, expiry assessments, and stability reviews to identify emerging risks, inform shelf-life decisions ...

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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?

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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.

QC Data Reviewer - LNP and Lipids

Boston, MA • On-site

Eurofins
Scientific Research and Development Services • 10K+ employees
Learn more about Eurofinsexternal

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Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 20 days ago

Eurofins rating

7.5

Company rating: 7.5 out of 10

Based on 181 frontline employees who took The Breakroom Quiz

64th of 121 rated laboratories

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.
Join us in shaping a safer, healthier, and more sustainable world. Explore opportunities with Eurofins and be part of a global team driving scientific excellence. Apply today and make a meaningful impact!
Job Description
This non-laboratory role is responsible for reviewing and evaluating analytical quality data for LNP formulations and lipid materials across stability studies, method development, and investigations. The role requires attention to detail, familiarity with GMP practices, and the ability to ensure data integrity and regulatory compliance.
  • 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 soundness, and appropriate corrective actions.
  • Verify calculations, data transcriptions, and chromatographic data for accuracy and compliance.
  • Ensure documentation adheres to GMP and applicable regulatory guidelines.
  • Maintain review timelines and tracking logs to support release and regulatory submission deadlines.
  • Partner with analytical and quality teams to resolve data discrepancies and review findings.
Qualifications
Minimum Required Qualifications:
  • B.S. in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field with 3-4 years of analytical laboratory experience in a GMP-regulated pharmaceutical or biopharmaceutical environment.
  • Proficiency in GMP regulations and Good Documentation Practices.
  • Understanding of how chromatography is operated and how to interpret the data
  • Strong organizational skills, attention to detail, and accuracy in documenting results.
  • Strong time management and multitasking abilities.
  • Ability to work independently and collaborate in a cross-functional environment.
  • Effective communication and documentation skills.
Preferred Qualifications:
  • Experience with chromatograms and the ability to interpret chromatographic data such as HPLC, UPLC, and LC-MS (experience with chromatography data review is a plus).
  • Familiarity with LNP and lipid technologies and investigations.
  • Experience with method development.
  • Experience with software systems such as SLIM, Veeva, JMP, and LIMS.
  • Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information
Additional Details:
The position is Full Time, Monday-Friday, 8am-5pm. Candidates currently living within a commutable distance of Boston, MA are encouraged to apply.
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
  • Annual rate is between $36.00-$40.00, depending on education and experience

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

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About Eurofins

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Industry

Scientific research and development services, biotechnology research and development and environmental consulting services

Company size

10,000+ Employees

Headquarters location

Leacock, PA, US

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