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Qc Stability Data Reviewer Jobs (NOW HIRING)

Lonza

QC Stability Coordinator

Tampa, FL · On-site

$18.75 - $25.75/hr

QC Stability Coordinator Location: Tampa, FL (on-site) Today, Lonza is a global leader in life ... You will monitor stability data, identify trends, and escalate out-of-specification or out-of-trend ...

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 ...

AMRI

Quality Control Data Reviewer III

Albany, NY · On-site

$84K - $104K/yr

The Data Reviewer III is responsible for supporting the manufacturing department, Stability ... The position will also support QA initiatives when necessary and collaborate with laboratory ...

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 ... The position will also support QA initiatives when necessary and collaborate with laboratory ...

Astrix Technology

Data Reviewer II/III

Albany, NY · On-site

Review QC testing and raw analytical data for accuracy, completeness, traceability, and compliance ... Review and trend stability data, prepare stability summary tables, and identify unexpected or ...

Pharmaron

Quality Control Data Reviewer I

Germantown, MD · On-site

$68K - $75K/yr

Quality Control Data Reviewer I Salary Range : $68,000- 75,000 Location : Germantown, MD About Pharmaron Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping ...

Astrix Inc

Data Reviewer II/III

Albany, NY · On-site

Review QC testing and raw analytical data for accuracy, completeness, traceability, and compliance ... Review and trend stability data, prepare stability summary tables, and identify unexpected or ...

Pharmaron

Quality Control Data Reviewer I

Germantown, MD · On-site

$68K - $75K/yr

Quality Control Data Reviewer ISalary Range: $68,000- 75,000Location: Germantown, MDAbout PharmaronPharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and ...

Curia, Inc.

Quality Control Data Reviewer II

Albany, NY · On-site

$72K - $89K/yr

Review quality control testing for compliance with internal SOPs and specifications * Assist in technical data review of the raw data generated for various compendial testing (such as USP/NF, EP, JP ...

Vaxcyte

Stability Manager

San Carlos, CA · On-site

$147K - $171K/yr

Produce impactful PowerPoint presentations to effectively communicate stability data to diverse ... Manages Quality Systems records for QC Stability- creates, assesses, reviews Deviations, Change ...

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Qc Stability Data Reviewer information

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How much do qc stability data reviewer jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for qc 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 QC Stability Data reviewer?

A QC Stability Data Reviewer is a quality control professional responsible for reviewing and verifying data generated from stability testing of pharmaceutical products. Their main role is to ensure the accuracy, completeness, and compliance of stability study data with regulatory requirements and company standards. They review analytical results, stability protocols, and reports to confirm that products remain safe and effective throughout their shelf life. This position often collaborates with laboratory analysts, quality assurance teams, and regulatory affairs to support product quality and regulatory submissions.

What are the key skills and qualifications needed to thrive as a QC Stability Data reviewer?

To thrive as a QC Stability Data Reviewer, you need a strong background in chemistry or life sciences, experience in quality control, and knowledge of regulatory guidelines such as GMP. Proficiency with laboratory information management systems (LIMS), chromatography data systems, and statistical analysis software is typically required. Attention to detail, critical thinking, and effective communication are standout soft skills for this position. These abilities ensure accurate data interpretation, regulatory compliance, and clear reporting in support of pharmaceutical product quality and stability.

What are common challenges faced by QC Stability Data reviewers, and how can they effectively address them?

QC Stability Data Reviewers often encounter challenges such as managing large volumes of complex stability data, ensuring data integrity, and meeting tight regulatory deadlines. Effective organization and attention to detail are essential, as is staying current with evolving regulatory requirements and company SOPs. Collaborating closely with laboratory analysts, quality assurance, and regulatory teams helps address discrepancies quickly and ensures data accuracy. Leveraging digital tools for data tracking and documentation can also streamline the review process and minimize errors.

What are popular job titles related to Qc Stability Data Reviewer jobs?

For Qc Stability Data Reviewer jobs, the most frequently searched job titles are:

Data Review Specialist, Quality Control

Bedford, MA • On-site

Ocular Therapeutix
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees
Learn more about Ocular Therapeutixexternal

Full-time

Re-posted 11 days ago

Job description

Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology, ELUTYX™. Ocular Therapeutix has built a robust product pipeline of drug delivery solutions developed to reduce the complexity and burden of the current standard of care and position itself to become a leader in the ophthalmic space.
Outside of the ophthalmic realm and behind the doors of our headquarters in Bedford, MA, we strive to build a strong culture where employees can flourish and achieve their career goals. We encourage out of the box thinking, cross-functional collaboration, and creativity.
Position Summary:
The Data Review Specialist will apply strong technical knowledge of laboratory operations, analytical data review, data integrity requirements, and quality systems to perform thorough reviews of analytical chemistry, microbiology, stability, and release testing data for accuracy, completeness, scientific soundness, and compliance with cGMP, GLP, and ALCOA+ expectations. This position is critical for supporting batch release, stability studies, environmental monitoring, method validation, and device testing.
In addition to data review, this role will support QC data monitoring activities, including evaluation of release data, raw material testing data, and stability data trends to identify emerging patterns, atypical results, potential OOT signals, and opportunities for improved product understanding. The Data Review Specialist will serve as a trusted partner to QC, QA, Stability, Manufacturing, Supply Chain, and Analytical Development stakeholders.
Key Responsibilities:
Quality Control Data Review
  • Review analytical raw data (HPLC/UPLC, GC, spectrophotometry, pH, dissolution, device function & performance testing) to ensure accuracy in calculations, instrument suitability, standards, sequences, and chromatographic integration.
  • Review microbiology data (bioburden, endotoxin, sterility, ID, EM, growth promotion, device-specific assays)
  • Review and support trending of stability data across applicable drug products, raw materials, and device-related attributes to identify emerging trends, atypical results, potential OOT signals, and data patterns requiring escalation.
  • Assist with interpretation of stability data in support of timepoint completion, stability reports, annual product reviews, regulatory submissions, and product lifecycle monitoring.
  • Support monitoring of released testing data for commercial and clinical batches, including review of assay, impurities/degradation products, dissolution/drug release, microbiological, and device performance data where applicable.
  • Collaborate with QC Stability, Raw Materials, QA, Manufacturing, Supply Chain, and Analytical Development to evaluate data trends and determine whether observed patterns require investigation, CAPA, procedural updates, or enhanced monitoring.
  • Support trending and monitoring of raw material data, including supplier lot-to-lot variability, retest/expiry data, CoA verification trends, and recurring analytical or documentation issues.

Documentation & Compliance
  • Ensure reviewed data packages meet cGMP, GLP, FDA/EMA, internal SOP, ALCOA+, and data integrity expectations for lot release, stability, raw materials, device testing, method validation, and regulatory support. Conduct timely and thorough review of data packages to support lot release, stability pulls, device testing, and method verification/validation activities.
  • Identify and document discrepancies, atypical results, potential data integrity concerns, and review comments; work with QC, QA, and originating groups to resolve issues in a timely manner.
  • Support OOS, OOT, deviations, CAPAs, audits, APR/PQR inputs, and regulatory requests by evaluating analytical, microbiological, stability, release, and raw material data for trends, anomalies, or potential root causes.

Quality Systems & Continuous Improvement
  • Recommend and support improvements to data review workflows, documentation templates, JPM, LIMS/Empower interfaces, Smartsheet trackers, and data integrity practices.
  • Generate and maintain reports, trackers, dashboards, and KPIs to support QC management review, workload visibility, product quality monitoring, and continuous improvement initiatives.
  • Serve as a technical resource to QC analysts by reinforcing best practices in documentation, audit trail review, ALCOA+ expectations, data monitoring, and inspection readiness

Cross-Functional Collaboration
  • Work cross-functionally with QC Chemistry, Raw Materials, Analytical Development, QC Microbiology, QA, Manufacturing, Supply Chain, and Product Development groups.
  • Communicate delays, data discrepancies, and potential risks to QC and QA leadership promptly.
  • Support cross-functional data requests related to product release, investigations, validations, or regulatory submissions.

Qualifications:
  • Bachelor's degree in Chemistry, Microbiology, Biochemistry, Biology, or related scientific discipline.
  • 5+ years in a QC laboratory, or data review role or a similar GMP-regulated environment, with a track record of strong performance, reliability, and increasing responsibility.
  • Strong working knowledge of cGMP, GLP, and data integrity expectations (ALCOA+).
  • Ability to independently review laboratory data, identify discrepancies, and collaborate effectively with peers and stakeholders to resolve issues in a timely manner.
  • Experience reviewing analytical chemistry and microbiology data (bioburden, endotoxin, EM trending, sterility).
  • Familiarity with chromatography software (e.g., Empower) and microbiology testing documentation.
  • Proficiency with electronic data management systems, including JPM, LIMS, Smartsheets and Empower.
  • Familiarity with statistical software, JMP preferred.
  • Prior experience with method validation and stability study protocols is a plus.

#LI-LM1
Salary Range
$98,000-$113,000 USD
Ocular Therapeutix is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws regarding nondiscrimination. Ocular Therapeutix provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, or status as a veteran. For information on how Ocular Therapeutix collects, stores, and utilizes candidate information please see our privacy policy found at https://www.ocutx.com/privacy-policy/. For the Privacy Notice for California Job Applicants, please see CCPA Applicant Notice.

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