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Per Diem Qc Data Reviewer Jobs (NOW HIRING)

Quality Control Data Reviewer

Milford, MA ยท On-site

$90K - $110K/yr

  • Medical

  • Retirement

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 ...

Quality Control Data Reviewer I

Germantown, MD ยท On-site

$68K - $75K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 ...

Quality Control Data Reviewer I

Germantown, MD ยท On-site

$68K - $75K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 ...

Ensure testing per deviations and laboratory investigations was followed. * Participate in required ... The QC Data Reviewer III is expected to operate within the framework of Tolmar's Core Values:

Data Reviewer III

Rensselaer, NY ยท On-site

  • Retirement

Verify calculations associated with testing are correctly done per procedures * Responsible to escalate OOS's identified in data review to the QC and QA leadership * Verify chromatography associated ...

QC Data Reviewer - LNP and Lipids

Boston, MA ยท On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This non-laboratory role is responsible for reviewing and evaluating analytical quality data for LNP formulations and lipid materials across stability studies, method development, and investigations.

QC Data Review Chemist

Oklahoma City, OK

$23 - $28/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

With moderate guidance, the Data Review Chemist II is responsible for utilizing the Quality Management System (QMS) standard operating procedures (SOP) and work instructions (WI) to perform quality ...

Review, evaluate, and accurately label audio recordings and other data files using designated software tools and quality control procedures. * Inspect, classify, and analyze data according to ...

Data Reviewer

Verona, WI ยท On-site

$35 - $43/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 ...

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Per Diem Qc Data Reviewer information

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$12

$26

$43

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

As of Aug 16, 2026, the average hourly pay for per diem 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 per diem QC data reviewer?

A Per Diem QC (Quality Control) Data Reviewer is a professional who works on a flexible, as-needed basis to review and verify data in quality control processes, often within pharmaceutical, biotechnology, or laboratory environments. Their main responsibility is to ensure the accuracy, completeness, and compliance of laboratory data with regulatory standards and company procedures. They may review test results, documentation, and reports to identify discrepancies or errors that could impact product quality or regulatory compliance. Per diem positions offer flexibility and are often used to support high workloads or special projects. These roles are critical in maintaining data integrity and ensuring that products meet required quality standards.

What is the difference between Per Diem Qc Data Reviewer vs Per Diem Data Coordinator?

AspectPer Diem Qc Data ReviewerPer Diem Data Coordinator
CredentialsTypically requires a degree in life sciences or related field, with experience in data reviewOften requires similar educational background, with focus on data management skills
Work EnvironmentWorks in clinical trial settings, reviewing data for accuracy and complianceManages data entry, organization, and coordination across trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsResearch organizations, clinical trial sponsors, CROs

The Per Diem Qc Data Reviewer primarily focuses on reviewing clinical data for quality and accuracy, while the Per Diem Data Coordinator handles data management and coordination tasks. Both roles require similar educational backgrounds and work within the clinical research industry, but their daily responsibilities differ significantly.

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

To thrive as a Per Diem QC Data Reviewer, you need strong analytical abilities, attention to detail, and a background in life sciences or a related field, often supported by a bachelor's degree. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practice (GMP) regulations, and relevant data review software is typically required. Excellent organizational skills, effective communication, and the ability to work independently are valuable soft skills for this role. These competencies ensure accurate data review, regulatory compliance, and reliable quality control in pharmaceutical or biotechnology environments.

What are some common challenges faced by per diem QC data reviewers and how can they be addressed?

Per Diem QC Data Reviewers often face challenges such as managing fluctuating work volumes, adapting to varying protocols across projects, and maintaining accuracy under tight deadlines. Since the role is typically flexible or on-call, time management and the ability to quickly familiarize oneself with new datasets or procedures are essential. To address these challenges, it helps to develop strong organizational skills, maintain up-to-date knowledge of quality standards, and communicate proactively with project managers and laboratory teams to clarify expectations and resolve discrepancies efficiently.
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Infographic showing various Per Diem Qc Data Reviewer job openings in the United States as of August 2026, with employment types broken down into 78% Full Time, and 22% Contract. Highlights an 100% In-person job distribution, with an average salary of $54,583 per year, or $26.2 per hour.

Quality Control Data Reviewer

Rentschler

Milford, MA โ€ข On-site

$90K - $110K/yr

Full-time

Medical, Retirement

Posted 14 days ago


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:
โ€ข Review and approval of QC test analytics; in process, release, stability, validation
โ€ข Track, organize, prepare QC test results for product release
โ€ข Review and approval of LIMS test results, labels and stage reports
โ€ข Revise SOPs, Forms
โ€ข 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.