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Qc Stability Data Reviewer Jobs (NOW HIRING)

Actalent

Data Reviewer

Verona, WI · On-site

$35 - $43/hr

You will collaborate with QC chemists to address any data or reporting issues and escalate ... Review method validation data for accuracy, integrity, and regulatory compliance. * Work with ...

Tolmar

QC Data Reviewer II (2nd Shift)

Fort Collins, CO · On-site

$32 - $34/hr

The QC Data Reviewer II is expected to operate within the framework of Tolmar's Core Values: * Center on People: We commit to support the well-being of our patients. We are committed to treating our ...

Tolmar

QC Data Reviewer II (2nd Shift)

Fort Collins, CO · On-site

The QC Data Reviewer II is expected to operate within the framework of Tolmar's Core Values: * Center on People: We commit to support the well-being of our patients. We are committed to treating our ...

Herbalife

Manager, Stability

Torrance, CA · On-site

... data review, statistical analysis, trending, and reporting. • Serve as a primary communication lead for stability, proactively updating project teams, QC managers, R&D, Regulatory, and regional ...

Eurofins

QC Data Reviewer - LNP and Lipids

Boston, MA · On-site

Review analytical data packages from stability studies, method development, and investigations for ... Partner with analytical and quality teams to resolve data discrepancies and review findings.

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Qc Stability Data Reviewer information

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$12

$26

$43

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:

Director, Quality Control

Redwood City, CA • On-site

Corcept Therapeutics
Biotechnology Research and Development • 51 - 200 employees
Learn more about Corcept Therapeuticsexternal

$215K - $253K/yr

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

The position will provide strategic and organizational leadership for the Quality Control function supporting Corcept's development and commercial programs. This position will have end-to-end oversight of all stability programs at contract laboratories and will author the stability sections of regulatory filings. This position will partner closely with the Sr Director of Analytical Development & Quality Control (ADQC) to continuously strengthen, expand, and scale the QC function, with increasing responsibility across broader QC activities.  

Responsibilities:

  • Lead the QC function with primary responsibility for the design, execution, and oversight of stability programs
  • Oversee stability studies conducted at external laboratories, ensuring compliance, data integrity, and timely execution
  • Review, trend, and maintain stability data. Alert the project team of any adverse trending
  • Collaborate with vendors and internal cross-functional teams to ensure that out-of-trend and out-of-specification results are addressed promptly
  • Provide stability study progress summaries to project teams and ensure that stability reports are completed promptly
  • Oversee internal documentation to support retest periods and shelf-life extension based on data generated from ongoing stability studies
  • Support analytical project leads in preparation of batch analysis; author and review stability sections required for regulatory submissions
  • Support analytical project leads in reviewing method validation protocols, reports, analytical method and test data
  • Manage data review qualifications of contract laboratories
  • Partner with the Sr Director of ADQC to build and enhance QC capabilities, infrastructure, and processes, with the expectation to progressively expand scope into broader QC oversight

Preferred Skills, Qualifications or Technical Proficiencies:

  • Strong technical expertise in stability study design, execution, and interpretation
  • Proven experience managing stability programs supporting late-stage development and global regulatory submissions
  • Experience in managing analytical testing in an outsourced environment
  • Experience in using statistical tools for data trend analysis and projection of drug substance retest period or drug product shelf-life
  • Excellent communication and collaboration skills with proven ability to work effectively with other functional groups

Preferred Education and Experience:

  • S. in relevant scientific discipline. Advanced degree in Analytical Chemistry or other relevant disciplines
  • 10+ years QC experience in the pharmaceutical industry

The pay range that the Company reasonably expects to pay for this headquarters-based position is $215,300-$253,200; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

 Applicants must be currently authorized to work in the United States on a full-time basis.

Apply