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Stability Data Reviewer Jobs (NOW HIRING)

Curia, Inc.

Quality Control Data Reviewer III

Albany, NY · On-site

$84K - $104K/yr

The Data Reviewer III is responsible for supporting the manufacturing department, Stability & Reference Standard department, and external customers. The principal responsibility of the Data Reviewer ...

AMRI

Quality Control Data Reviewer III

Albany, NY

$84K - $104K/yr

The Data Reviewer III is responsible for supporting the manufacturing department, Stability & Reference Standard department, and external customers. The principal responsibility of the Data Reviewer ...

Astrix Inc

Data Reviewer II/III

Albany, NY · On-site

Review and trend stability data, prepare stability summary tables, and identify unexpected or inconsistent results. * Conduct electronic data reviews and signatures while ensuring complete and ...

Astrix Inc

Data Reviewer II/III

Albany, NY · On-site

Review and trend stability data, prepare stability summary tables, and identify unexpected or inconsistent results. * Conduct electronic data reviews and signatures while ensuring complete and ...

Curia, Inc.

Data Reviewer III

Rensselaer, NY · On-site

Format and review Stability summary tables, Stability Protocols for accuracy and compliance with current Curia formats * Enter data into Stability summary tables. Perform tracking and trending of ...

curiate.co

Data Reviewer III

Rensselaer, NY · On-site

Format and review Stability summary tables, Stability Protocols for accuracy and compliance with current Curia formats * Enter data into Stability summary tables. Perform tracking and trending of ...

Curia, Inc.

Data Reviewer III

Rensselaer, NY · On-site

Format and review Stability summary tables, Stability Protocols for accuracy and compliance with current Curia formats * Enter data into Stability summary tables. Perform tracking and trending of ...

AMRI

Data Reviewer III

Rensselaer, NY

Format and review Stability summary tables, Stability Protocols for accuracy and compliance with current Curia formats * Enter data into Stability summary tables. Perform tracking and trending of ...

AMRI

Data Reviewer III

Rensselaer, NY

Format and review Stability summary tables, Stability Protocols for accuracy and compliance with current Curia formats * Enter data into Stability summary tables. Perform tracking and trending of ...

Eurofins

Stability Data Specialist

Lexington, MA · On-site

$31 - $35/hr

Review and interpret analytical data with client support; contribute to technical reports and ... Build and manage stability studies within validated systems, as applicable. * Ensure GMP data ...

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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?

States with the most job openings for Stability Data Reviewer jobs include:

What are popular job titles related to 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.

Quality Control Data Reviewer III

Albany, NY • On-site

Curia, Inc.
Pharmaceutical and Medicine Manufacturing • 1 - 5K employees
Learn more about Curia, Inc.external

$84K - $104K/yr

Full-time

Retirement

Re-posted 20 days ago

Curia rating

7.6

Company rating: 7.6 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

Job description


Data Reviewer III in Albany, NY
Build your future at Curia, where our work has the power to save lives.
The Data Reviewer III is responsible for supporting the manufacturing department, Stability & Reference Standard department, and external customers. The principal responsibility of the Data Reviewer III is the review and approval of primary analytical data according to cGMP guidelines. The Data Reviewer will be expected to review analytical data including XRPD, PSD, DSC, TGA, UV, FTIR, HPLC, KF, USP testing for compliance and completeness against established SOPs, methods and procedures. The position will also support QA initiatives when necessary and collaborate with laboratory personnel to review data per cGMP compliance and data integrity. The Reviewer should incorporate sound judgement, critical thinking, and cGMP principles to ensure the integrity of the data meet acceptable quality standards. In addition, the Reviewer will provide appropriate guidance to analysts, supervisors, and quality personnel to promote compliance for our customers.
Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives.
We proudly offer
  • Generous benefit options (eligible first day of employment)
  • Paid training, vacation and holidays (vacation accrual begins on first day of employment)
  • Career advancement opportunities
  • Education reimbursement
  • 401K program with matching contributions
  • Learning platform
  • And more!

Responsibilities
  • Responsible for technical data review of the raw data generated for various compendial testing (such as USP/NF, EP, JP, etc.) as well as Curia In-house and client methodologies for various client projects to ensure data accuracy and integrity
  • Must have working knowledge and understanding of various analytical instrumentation including but not limited to Gas Chromatography (GC), High-performance liquid chromatography (HPLC/UHPLC), ICP-MS, Infrared spectroscopy (IR), Differential scanning calorimeter (DSC), UV-Vis, Karl-Fischer auto titrator, Optical rotation, Dissolution, etc.
  • Trend stability data to ensure consistency with historical timepoints and no unexpected results
  • Verify calculations associated with Stability samples/Reference standards/Raw Materials/Intermediates testing are correctly done
  • Format and review Stability summary tables, Stability Protocols for accuracy and compliance with current Curia formats
  • Enter data into Stability summary tables. Perform tracking and trending of data as requested. Compile data and provide data summaries to management
  • Collaborate with lab personnel for data review per cGMP compliance, data integrity
  • Perform electronic review and signatures while reviewing electronic data
  • Verify for traceability of samples, standards, reagents, instruments etc.
  • Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed
  • Ensure the testing data received from external labs are reviewed per site procedures
  • Make sure all tests are per cGMP compliance and in compliance with the company's standard operating procedures
  • Provide support on QA initiatives (Investigations, change controls etc.) when necessary
  • Review and approve test methods, SOPs, forms, and other documents as necessary
  • Support supervisors in OOS Investigations and complete CAPA requirements
  • Participate in customer technical discussions for analytical issues
  • Interact with outside departments including attending meetings, providing updates, etc.
  • Coordinate testing performed at contract testing labs for stability samples etc.
  • Provide training to new hires as needed. Attend internal and external training on related subjects, cGMP compliance and data integrity, new techniques and procedures
  • Provide guidance to lower level Data Reviewers as needed

Qualifications
  • Bachelor's Degree in Chemistry or related field and a minimum of five years' relevant industry experience; OR
  • Master's degree and three years' relevant experience

Preferred
  • Experience working in cGMP or GLP pharmaceutical industry environment

Other Qualifications
  • Must pass a background check
  • Must pass a drug screen
  • May be required to pass Occupational Health Screening

Pay Range: $84,000-$104,824/yr.
Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.
All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is 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 on the basis of disability. Curia is an E-Verify employer.
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