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Qc Data Reviewer Jobs in California (NOW HIRING)

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 ...

QC & Data Analyst

Covina, CA · On-site

$25 - $28/hr

We are actively hiring a QC & Data Analyst to support our Covina, CA site. LOCATION : Onsite FLSA ... Conduct a thorough and precise review of study charts utilizing SOPs, policies, GCP, GDP, and ...

We are actively hiring a QC & Data Analyst to support our Covina, CA site. LOCATION : Onsite FLSA ... Conduct a thorough and precise review of study charts utilizing SOPs, policies, GCP, GDP, and ...

QC & Data Analyst

Covina, CA · On-site

$25 - $28/hr

We are actively hiring a QC & Data Analyst to support our Covina, CA site. LOCATION : Onsite FLSA ... Conduct a thorough and precise review of study charts utilizing SOPs, policies, GCP, GDP, and ...

We provide quality resources in four specialty areas: Information Technology (IT), Clinical ... Ability to review data across multiple documents for consistency. The candidate must be able to ...

Assists with QC's data management, including data review and trending. * Maintains specific QC files and database records for process and/or quality improvement efforts. * Maintain laboratory ...

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Qc Data Reviewer information

See California salary details

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How much do qc data reviewer jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for qc data reviewer in California is $25.90, according to ZipRecruiter salary data. Most workers in this role earn between $14.23 and $35.82 per hour, depending on experience, location, and employer.

What is a qc data reviewer?

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 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.

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 most commonly searched types of Qc Data Reviewer jobs in California?

The most popular types of Qc Data Reviewer jobs in California are:

What are popular job titles related to Qc Data Reviewer jobs in California?

For Qc Data Reviewer jobs in California, the most frequently searched job titles are:

What job categories do people searching Qc Data Reviewer jobs in California look for?

The top searched job categories for Qc Data Reviewer jobs in California are:

What cities in California are hiring for Qc Data Reviewer jobs?

Cities in California with the most Qc Data Reviewer job openings:

Infographic showing various Qc Data Reviewer job openings in California as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, and 2% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $53,869 per year, or $25.9 per hour.

Data Reviewer, Quality Control

Avid Bioservices

Tustin, CA

$32.30 - $40.38/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 13 days ago


Job description

Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Your Role:
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 Empower and SoftMax Pro software including but not limited to contents, results, data accuracy, and scientific relevance, format and adherence to cGMPs.
  • Perform a thorough review of raw data, including electronic raw data and documentations to ensure compliance with applicable specifications and/or protocols.
  • Conduct GMP review of laboratory notebooks, logbooks, and associate forms.
  • Conduct GMP review of electronic raw data to ensure compliance with data integrity policies.
  • Support OOS/OOT investigations.
  • Support internal and external audit.
  • Support QC method validation review, as needed.
  • Perform review of procedural and method revisions, where necessary.
  • Perform other duties as assigned to support Quality activities.
Minimum Qualifications:
  • Bachelor's degree, preferably in a life sciences field (such as biology, microbiology, biochemistry, chemistry).
  • 4+ years' work experience in a GMP/biopharmaceutical/pharmaceutical manufacturing environment.
  • Experience with Empower and SoftMax Pro software.
  • Knowledge of cGMPs, pharmacopeia and compendial requirements.
  • Experience in and knowledge of 21 CFR data integrity requirements.
  • Familiarity with analytical testing methods and validation including laboratory instrumentation.
  • Strong verbal and written communication skills.
  • Familiarity with laboratory computerized systems such as Empower and LIMS.
  • Proficient with Microsoft applications.
Position Type/Expected Hours of Work:
This role is a full-time position. Days and hours of work are Monday through Friday, 8:00 a.m. to 5 p.m. unless otherwise stated by Supervisor. Must be available to work holidays, weekends, or extended hours if needed.
Compensation:
We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
The compensation range for this role is $32.30-$40.38 hourly, depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
Who you are:
  • You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
  • Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
  • You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
  • You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.
Physical Demands & Work Environment:
In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.
Employment Type: Full-Time