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Full Time Qc Data Reviewer Jobs (NOW HIRING)

Rentschler

Quality Control Data Reviewer

Milford, MA · On-site

$90K - $110K/yr

As part of the Milford site's Quality Control team, the Data Reviewer is responsible for the cGMP analytical data review and documentation generated during laboratory analysis in the quality control ...

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 ...

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 ...

Kelly Services

QC Data Reviewer - Bristol PA

Bristol, PA · On-site

$40 - $60/hr

Kelly ® Science & Clinical is seeking a 2 QC Data Reviewers for a contract position (minimum 4 months, with potential to convert to full-time) at a premier client in Bristol, PA. If you're ...

Curia, Inc.

Quality Control Data Reviewer III

Albany, NY · On-site

$84K - $104K/yr

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 ...

CEDENT

Data Reviewer, Quality Control

Verona, WI

The Data Reviewer is responsible for ensuring the completion, quality, and compliance of laboratory data and reports produced within the Quality Control (QC) team. This includes the technical review ...

Curia, Inc.

Data Reviewer III

Rensselaer, NY · On-site

Quality Control Data Reviewer III - Onsite position in Rensselaer, NY Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing ...

Nitto Denko Corp.

$91K - $111K/yr

The individual provide The QC data reviewer assists in writing investigations and CAPAs and works with Quality Assurance to ensure timely release and closure of all stability batches. This is a 2nd ...

Thorne

Quality Control Data Associate

Summerville, SC · On-site

Lab Employment Type: Full Time Location: Summerville, SC Reporting To: Jordan Smith Description At ... Assemble, review, and maintain Quality Control laboratory data to support accurate product ...

Thorne

Quality Control Data Associate

Summerville, SC · On-site

Assemble, review, and maintain Quality Control laboratory data to support accurate product disposition and timely material release. * Generate Certificates of Analysis (COAs) and other quality ...

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Full Time Qc Data Reviewer information

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How much do full time qc data reviewer jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for full time 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 does a full time QC data reviewer do?

A Full Time QC (Quality Control) Data Reviewer is responsible for reviewing and verifying data generated during laboratory testing or production processes to ensure accuracy, completeness, and compliance with regulatory standards. They check documentation, identify errors or inconsistencies, and work with laboratory staff to resolve issues before final data approval. The role is crucial in industries such as pharmaceuticals, biotechnology, and food manufacturing, where data integrity and regulatory compliance are critical. QC Data Reviewers help maintain high-quality standards and support audits or inspections by ensuring all records are accurate and up to date.

What are the key skills and qualifications needed to thrive as a full time QC data reviewer?

To thrive as a Full Time QC Data Reviewer, a strong background in data analysis, attention to detail, and familiarity with quality control standards—often supported by a degree in life sciences or a related field—is essential. Proficiency with laboratory information management systems (LIMS), data review software, and knowledge of regulatory guidelines like GMP or GLP is typically required. Excellent organizational skills, critical thinking, and effective communication help ensure accuracy and timely reporting. These skills and qualities are crucial for maintaining data integrity, regulatory compliance, and the overall reliability of scientific or manufacturing processes.

What are some common challenges faced by full time QC data reviewers, and how can these be managed effectively?

Full Time QC Data Reviewers often encounter challenges such as tight deadlines, managing large volumes of data, and ensuring strict compliance with regulatory standards. These challenges can be managed by maintaining strong organizational skills, staying updated on quality guidelines, and leveraging digital tools to streamline the review process. Additionally, effective communication with laboratory analysts and other quality teams is essential to quickly resolve discrepancies and maintain data integrity.

What is the difference between Full Time Qc Data Reviewer vs Clinical Data Coordinator?

AspectFull Time Qc Data ReviewerClinical Data Coordinator
CredentialsTypically requires a degree in life sciences or related field, often with certifications like CDMP or CDISCRequires a degree in health sciences, nursing, or related fields; certifications may include CDISC or clinical research certifications
Work EnvironmentWorks in clinical trial settings, reviewing data quality and consistencyCoordinates data collection, entry, and management in clinical research projects
Employer & IndustryPharmaceutical companies, CROs, biotech firmsResearch institutions, hospitals, pharmaceutical companies

While both roles involve clinical data, the Full Time Qc Data Reviewer primarily focuses on reviewing and ensuring data quality, whereas the Clinical Data Coordinator manages data collection and entry processes. The reviewer ensures data accuracy, while the coordinator oversees data flow and compliance throughout the trial.

What cities are hiring for Full Time Qc Data Reviewer jobs?

Cities with the most Full Time 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 are popular job titles related to Full Time Qc Data Reviewer jobs?

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

Full Time Qc Data Reviewer jobs near you

Quality Control Data Reviewer

Milford, MA • On-site

Rentschler
See more jobs at Rentschlerexternal

$90K - $110K/yr

Full-time

Medical, Retirement

Re-posted 10 days ago

Key responsibilities

  • Review and approve cGMP analytical data to ensure accuracy and compliance with specifications, SOPs, and standards

  • Track, organize, and prepare QC test results for product release and review LIMS test results, labels, and stage reports

  • Support product release activities, resolve quality issues, and assist in revising SOPs and test forms

Job description

Advancing medicine to save lives. Together.
Thanks to many decades of experience and our passion for what we do, we make an essential contribution to the global availability of biopharmaceuticals, especially for patients with rare and serious diseases.
Rentschler Biopharma SE is a leading contract development and manufacturing organization (CDMO) focused exclusively on client projects. We offer customized full-service solutions for bioprocess development and the production of complex biopharmaceuticals. As a German family-owned company with an international footprint and global reach, we combine experts, expertise and years of experience to develop best-in-class solutions - together with our clients.
Rentschler Biopharma has approximately 1,400 employees and is headquartered in Laupheim, Germany, with a site in Milford, MA, USA. In 2024, we joined the United Nations Global Compact, underlining our commitment to sustainability.
As an independent family-owned company, we live by the motto: Many hands, many minds - ONE TEAM! Open, respectful cooperation characterizes our working environment, where quality awareness, diligence and responsibility are our top priorities. With all the diversity of our talents in the Rentschler team, we pursue one vision together: advancing medicine to save lives.
As part of the Milford site's Quality Control team, the Data Reviewer is responsible for the cGMP analytical data review and documentation generated during laboratory analysis in the quality control laboratory. 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 release
• Review and approval of LIMS test results, labels and stage reports
• Revise SOPs, Forms
• Train employees on cGMP/GDP
Duties and Responsibilities
  • Review and approval of cGMP analytical data comparing results to internal and customer specifications, SOPs, and established standards to ensure accuracy and quality of data
  • Works collaboratively with QC team members and cross functional teams for timely resolution of quality issues to achieve project goals
  • Support Product Release activities ensuring timelines are met
  • Work on problems of diverse scope in which analysis of data requires evaluation of identifiable factors
  • Identify and resolve issues with assistance from Data Review team
  • Review of LIRs
  • Support all data integrity initiatives and strive for right first time
  • Make daily decisions about the quality of data based on biochemical knowledge and compliance background
  • Revise, create SOPS and/or test forms as required
  • Assists with metrics for trending and reporting as required, stability and QC analytical data
  • Task and team-oriented, analytical, organized, detail-oriented, self-motivated and ability to multitask
  • Exceptional communication and interpersonal skills
  • Assists in training of new hires and retraining of QC laboratory staff, as needed
  • Assist/mentor QC new hires on cGMP/GDP
  • Strong knowledge of QC analytical equipment and software required
  • Strong communications skills - written and verbal
  • Able to prioritize workload to meet stringent timelines
  • Provide timely status updates to Management upon request
  • Proficient with MS Outlook, Word, Excel and PowerPoint, and other electronic systems
  • Performs other duties as assigned

Qualifications
  • B.S. in Chemistry, Biology, Chemical Engineering, or related biological sciences
  • 3+ years in a cGMP analytical laboratory environment
  • HPLC, PA800, CS2500, SDS Page
  • LIMS, EMPOWER
  • cGMP experience

Working Conditions
  • Personal protective equipment must be worn in the laboratories according to Rentschler safety requirements
  • Will interact with other departments
  • Pace may be fast and job completion demands may be high
  • Not a hybrid position, work must be performed on site

Physical Requirements
  • May be required to stand for long periods of time while performing review of lab logbooks, equipment, lab documentation
  • Must be able to walk distances between labs, offices, departments
  • Must be able to work safely in a lab environment
  • PPE as required

Base Pay Range
$90,000 - $110,000
Disclosure Statement
Rentschler Biopharma, Inc is committed to fair and equitable compensation practices. The base pay range listed for this position is the anticipated annual base salary range the organization reasonably, and in good faith, expects to pay for this position at this time. Actual compensation is determined based on several factors that may include seniority, education, training, relevant experience, relevant certifications, geography of work location, job responsibilities, or other application factors permissible by law. The annual base salary is just one component of our Total Rewards package, which also includes our annual discretionary bonus program, medical insurance, our generous 401K program, plus a host of other benefits to aligned to support our employees' personal and professional wellness. The salary pay range is subject to change and may be modified at any time.

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