ZipRecruiter

Log In

1

Qc Data Reviewer Jobs (NOW HIRING)

AllSTEM Connections

Quality Control Analyst

Rensselaer, NY · On-site

$64.50K - $97.80K/yr

Review analytical QC data, compile trend reports, and provide technical summaries to management to ensure manufacturing accuracy. • Audit Readiness: Maintain a pristine, compliant workspace and ...

Frontage Laboratories

QC Manager

Exton, PA · On-site

The QC Manager leads a team of QC reviewers responsible for data verification, review of assay outputs, documentation accuracy, and compliance across all GLP bioanalytical studies. Key ...

INCOG

QC Compliance Specialist, 3rd Shift

Fishers, IN · On-site

The Quality Control Compliance Specialist plays a vital role on the QC team with analytical and ... Perform in-depth technical data review of all analytical and microbiological testing performed on ...

TapestryHealth

Data Quality Reviewer(CCM)

NY · Remote

$18 - $20/hr

In this role, you will review patient data in accordance with established guidelines to ensure it is complete, accurate, and ready for advanced practice providers to develop care plans for patients.

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 ... control. As a Field Inspector covering Salt Lake County, you will perform residential occupancy ...

Moderna Therapeutics

$20 - $25.50/hr

Coaching and guiding QC staff through QA lab walkthroughs, real-time data reviews, and training support. * Maintaining robust oversight of stability programs and lifecycle management of reference ...

Twist BioScience

Responsibilities • Review and release products based on established QC metrics • Monitor QC data • Investigate product/process/quality issues • Review of CAPAs, process deviations, root cause ...

Far Inspections

Occupancy Data Reviewer

Lawton, OK · On-site

$25 - $35/hr

FAR Inspections is a leading provider of property data for mortgage lenders nationwide. Based in ... control. As a Field Inspector covering Comanche County, you will perform residential occupancy ...

Tapestryhealth

Data Quality Reviewer(CCM)

NY · On-site +1

$18 - $20/hr

In this role, you will review patient data in accordance with established guidelines to ensure it is complete, accurate, and ready for advanced practice providers to develop care plans for patients.

Microbac

Quality Assurance Specialist

Northbrook, IL · On-site

$46.50K - $56K/yr

Serves as the focal point for QA/QC and is responsible for the oversight and/or review of quality control data such as data, control charts, calibration records, and other QA/QC data. KEY ...

next page

Showing results 1-20

People also search for

All JobsQc Data Reviewer Jobs

Qc Data Reviewer information

See salary details

$12

$26

$43

How much do qc data reviewer jobs pay per hour?

As of Jun 1, 2026, the average hourly pay for qc 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 Data Reviewer job?

A QC Data Reviewer is responsible for reviewing laboratory data, documents, and reports to ensure accuracy, compliance with regulatory guidelines, and adherence to standard operating procedures. They verify analytical results, identify discrepancies, and ensure data integrity before final approval. This role is critical in pharmaceutical, biotechnology, and manufacturing industries to maintain product quality and regulatory compliance.

What are the key skills and qualifications needed to thrive in the Qc Data Reviewer position, and why are they important?

To excel as a QC Data Reviewer, candidates typically require a background in life sciences, strong analytical skills, attention to detail, and experience in quality control processes. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practice (GMP) guidelines, and relevant data analysis tools or software is often expected. Excellent communication, critical thinking, and organizational skills help reviewers share findings effectively and manage competing priorities. These capabilities ensure data integrity, regulatory compliance, and consistent quality in highly regulated environments.

What are the typical day-to-day responsibilities for a QC Data Reviewer?

A QC Data Reviewer is responsible for reviewing laboratory data, checking for accuracy and compliance with internal and regulatory standards, and verifying that test results meet established criteria. They often collaborate with lab analysts, quality assurance teams, and supervisors to resolve discrepancies and clarify data issues. Daily tasks may include evaluating raw data sets, preparing reports, participating in audits, and assisting in process improvements. This role is essential to ensure that only high-quality, compliant data is released for product decisions, contributing to the overall reliability and reputation of the organization.
More about Qc Data Reviewer jobs
What cities are hiring for Qc Data Reviewer jobs? Cities with the most Qc Data Reviewer job openings:
What are the most commonly searched types of Qc Data Reviewer jobs? The most popular types of Qc Data Reviewer jobs are:
What states have the most Qc Data Reviewer jobs? States with the most job openings for Qc Data Reviewer jobs include:
What job categories do people searching Qc Data Reviewer jobs look for? The top searched job categories for Qc Data Reviewer jobs are:
Qc Data Reviewer jobs near you
Infographic showing various Qc Data Reviewer job openings in the United States as of May 2026, with employment types broken down into 92% Full Time, 4% Contract, and 4% Nights. Highlights an 100% In-person job distribution, with an average salary of $54,583 per year, or $26.2 per hour.
Quality Control Specialist, Analytical

Quality Control Specialist, Analytical

Capricor Therapeutics

San Diego, CA

Full-time

Posted 22 days ago

Job description

Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.

The QC Specialist, Analytical supports the quality and compliance of cell therapy programs through a focus on data review, investigations, and quality systems. This role plays a key part in ensuring that QC methods, analytical data, and documentation meet cGMP requirements and regulatory expectations for clinical and commercial manufacturing. Working cross-functionally with Quality Assurance, Analytical Development, and Manufacturing, this position emphasizes technical writing, data analysis, and product quality oversight. While maintaining a strong understanding of laboratory operations, the role is not primarily focused on routine bench work.

Responsibilities
  • Lead and support investigations related to deviations, OOS/OOT/invalid results, and CAPAs, ensuring thorough root cause analysis and clear documentation.
  • Review QC data, laboratory records, and analytical results to assess product impact and ensure compliance with cGMP standards.
  • Author and review SOPs, test methods, validation protocols/reports, and investigation summaries.
  • Perform data trending and analysis to identify variability, shifts, or emerging risks in QC and product quality data.
  • Support method lifecycle activities including qualification, validation, transfer, and periodic review in collaboration with Analytical Development.
  • Provide technical oversight of QC methods to ensure they remain scientifically sound and fit for purpose.
  • Contribute to change control activities and assess potential impact to product quality and method performance.
  • Support maintenance of product specifications, including acceptance criteria and scientific justification.
  • Participate in stability program activities, including data review and trending to support shelf-life determinations.
  • Ensure accurate, complete, and compliant GMP documentation in alignment with data integrity (ALCOA+) principles.
  • Support audits and regulatory inspections by preparing and reviewing technical documentation.
  • Collaborate cross-functionally with QA, Manufacturing, and external partners to support product quality objectives.
  • Contribute to quality risk assessments (ICH Q9), continuous improvement initiatives, and quality system enhancements.
Required Qualifications (Must‑Haves)
  • Bachelor’s degree in Life Sciences, Biotechnology, or related field (advanced degree preferred).
  • ~5–8+ years of experience in GMP Quality Control, Quality Assurance, or related function within biotech or pharmaceutical industry.
  • Strong knowledge of cGMP, FDA/EMA regulations, and ICH guidelines.
  • Experience with deviation investigations, OOS/OOT, CAPAs, and change control processes.
  • Strong technical writing, data analysis, and problem-solving skills.
  • Working knowledge of analytical methods such as flow cytometry, PCR, ELISA, and bioassays.
  • Excellent communication skills and ability to collaborate in a cross-functional environment.
  • High attention to detail and commitment to quality and compliance.
Work Environment & Physical Requirements
  • Primarily office-based with occasional presence in laboratory or manufacturing areas as needed.
  • Ability to sit or stand for extended periods and move throughout the facility.
  • Ability to gown and enter classified areas when required.
  • Ability to lift and carry up to 40 lbs as needed.
Why Capricor?
Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.

Come Work With Us!
At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.

Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.



Notice to Recruiting Agencies
Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.