1

Quality Control Reviewer Jobs (NOW HIRING)

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 ...

New

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 ...

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 ...

Data Reviewer, Quality Control

Tustin, CA · On-site

$32.30 - $40.38/hr

The Data Reviewer, Quality Control 's main responsibility will be to review Quality Control analytical data. In this role you will: * Conduct a comprehensive and critical evaluation on QC data in ...

Data Reviewer, Quality Control

Tustin, CA · On-site

$31.63 - $42.16/hr

The Data Reviewer, Quality Control 's main responsibility will be to review Quality Control analytical data. In this role you will: * Conduct a comprehensive and critical evaluation on QC data in ...

... control reviews of task order plans and specifications developed by planning and estimating staffConduct final reviews of completed work to verify quality of final product, code compliance, and work ...

Perform quality control reviews of task order plans and specifications developed by planning and estimating staff * Conduct final reviews of completed work to verify quality of final product, code ...

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 ...

New

Showing results 21-40

Quality Control Reviewer information

See salary details

$30.5K

$81.3K

$129.5K

How much do quality control reviewer jobs pay per year?

As of Aug 7, 2026, the average yearly pay for quality control reviewer in the United States is $81,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $100,000.00 per year, depending on experience, location, and employer.

What are some common challenges faced by quality control reviewers and how can they be addressed?

Quality Control Reviewers often encounter challenges such as handling high volumes of detailed work within tight deadlines and ensuring consistent application of standards across diverse projects. To address these, strong organizational skills and effective time management are crucial. Collaborating closely with other team members, such as production staff or project managers, helps clarify requirements and maintain quality benchmarks. Regular calibration meetings and ongoing training also support consistency and accuracy in reviews.

What is a quality control reviewer?

Quality Control Reviewers are professionals responsible for ensuring that products, documents, or processes meet established quality standards and regulatory requirements. They review work for accuracy, completeness, and compliance, often using checklists or guidelines to identify errors or inconsistencies. Their role is critical in industries like manufacturing, healthcare, and finance, where maintaining high quality is essential to safety and customer satisfaction. Quality Control Reviewers often provide feedback and recommend improvements to help organizations achieve better outcomes.

What are the key skills and qualifications needed to thrive as a quality control reviewer?

To thrive as a Quality Control Reviewer, you need strong analytical skills, attention to detail, and a background in quality assurance or a relevant field, often supported by a bachelor’s degree. Familiarity with industry-specific quality standards, reporting tools, and data analysis systems like ISO, Six Sigma, or specialized QC software is typically required. Exceptional communication, problem-solving abilities, and a proactive mindset set outstanding reviewers apart. These skills ensure that products or services consistently meet required standards, reducing errors and maintaining organizational reputation.

What is the difference between Quality Control Reviewer vs Quality Assurance Specialist?

AspectQuality Control ReviewerQuality Assurance Specialist
CertificationsOften requires certifications like ASQ CQE or related quality certificationsTypically requires similar certifications, with additional focus on process improvement
Work EnvironmentPrimarily inspects products or processes in manufacturing or production settingsFocuses on developing and implementing quality systems across various departments
Employer & Industry UsageCommon in manufacturing, production, and industrial sectorsUsed across manufacturing, healthcare, and service industries
Search & Comparison IntentPeople compare to understand inspection roles and certificationsPeople compare to learn about quality system development and process improvement

The main difference is that a Quality Control Reviewer primarily inspects products and ensures they meet quality standards, while a Quality Assurance Specialist develops and maintains quality systems to prevent defects. Both roles require similar certifications and are common in manufacturing industries, but their focus areas differ—inspection versus process improvement.

Who can be a quality control reviewer?

A quality control reviewer is typically someone with attention to detail, good communication skills, and knowledge of quality standards relevant to the industry. They often have a background in the specific field, such as manufacturing, healthcare, or software, and may require training or certifications related to quality assurance processes.

How to get into a quality control reviewer with no experience?

To become a quality control reviewer with no experience, focus on developing attention to detail, basic knowledge of quality standards, and familiarity with inspection tools. Entry-level positions often require a high school diploma or equivalent, and gaining relevant skills through online courses or certifications can improve your chances. Gaining experience in related roles or industries can also help you qualify for quality control reviewer positions.
More about Quality Control Reviewer jobs
What cities are hiring for Quality Control Reviewer jobs? Cities with the most Quality Control Reviewer job openings:
What states have the most Quality Control Reviewer jobs? States with the most job openings for Quality Control Reviewer jobs include:
Infographic showing various Quality Control Reviewer job openings in the United States as of August 2026, with employment types broken down into 83% Full Time, and 17% Part Time. Highlights an 75% In-person, 8% Hybrid, and 17% Remote job distribution, with an average salary of $81,324 per year, or $39.1 per hour.

Quality Control Data Reviewer

Rentschler

Milford, MA • On-site

$90K - $110K/yr

Other

Medical, Retirement

Posted 3 days ago

New


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.