QC Data Reviewer

Jobot; Costa Mesa (CA); On-site; USD 44,000 - 55,000; Full time

Job summary

Jobot is seeking a QC Data Reviewer to support a GMP-regulated analytical chemistry laboratory in Costa Mesa, CA. The role focuses on reviewing laboratory data and testing records for accuracy, completeness, and compliance, enabling product release, stability testing, and manufacturing support.

Ideal candidates have 3–5 years in GMP QC labs and familiarity with HPLC, UV-Vis, pH and related methods, along with GxP software tools such as LabX, Chromeleon, or Cary WinUV.

Qualifications

• 3–5 years of experience in a pharmaceutical, biotechnology, or GMP-regulated QC laboratory.
• Experience reviewing analytical data, test results, or GMP laboratory documentation.
• Knowledge of cGMP, Good Documentation Practices, and data integrity principles.
• Familiarity with analytical techniques such as HPLC, UV-Vis, pH, osmolality, water content, conductivity, TOC, and compendial testing.
• Familiarity with laboratory software such as LabX, Chromeleon, or Cary WinUV.
• Bachelor’s degree in chemistry, biochemistry, or a related scientific field preferred; equivalent relevant experience will be considered.

Responsibilities

• Review analytical raw data, logbooks, calculations, and supporting documentation.
• Review electronic laboratory data, chromatograms, and audit trails.
• Verify results against approved specifications, test methods, and procedures.
• Confirm documentation follows cGMP, Good Documentation Practices, and data integrity requirements.
• Identify discrepancies and work with QC analysts and supervisors to resolve them.
• Escalate atypical, out-of-specification, or out-of-trend results according to established procedures.
• Complete assigned reviews within required timelines.

Skills

Attention to detail

Prioritization

Education

Bachelor’s degree in chemistry/biochemistry or related field

Tools

LabX

Chromeleon

Cary WinUV

Job description

QC Data Reviewer

$32 - $40 per hour | Costa Mesa, CA | On-site | Consulting

A bit about us:

We’re a growing contract development and manufacturing organization that partners with biopharmaceutical companies from early-stage process development through commercial manufacturing.

Why join us?

• Join a growing life sciences organization supporting the development and manufacturing of products that make a meaningful impact.
• Take ownership of supply chain strategy, procurement, vendor management, inventory, and material planning.
• Work closely with leadership and cross-functional teams across Manufacturing, Quality, Business Development, and Project Management.
• Help improve processes, reduce costs, and build a more efficient and scalable supply chain operation.
• Be part of a quality-driven environment that values accountability, collaboration, safety, and continuous improvement.

Job Details

We’re looking for a QC Data Reviewer to support a GMP-regulated analytical chemistry laboratory. This person will review laboratory data and testing records for accuracy, completeness, and compliance, supporting manufacturing, product release, and stability testing.

Responsibilities

• Review analytical raw data, logbooks, calculations, and supporting documentation.
• Review electronic laboratory data, chromatograms, and audit trails.
• Verify results against approved specifications, test methods, and procedures.
• Confirm documentation follows cGMP, Good Documentation Practices, and data integrity requirements.
• Identify discrepancies and work with QC analysts and supervisors to resolve them.
• Escalate atypical, out-of-specification, or out-of-trend results according to established procedures.
• Complete assigned reviews within required timelines.

Qualifications

• Approximately 3–5 years of experience in a pharmaceutical, biotechnology, or GMP-regulated QC laboratory.
• Experience reviewing analytical data, test results, or GMP laboratory documentation.
• Working knowledge of cGMP, Good Documentation Practices, and data integrity principles.
• Familiarity with analytical techniques such as HPLC, UV-Vis, pH, osmolality, water content, conductivity, TOC, and compendial testing.
• Familiarity with laboratory software such as LabX, Chromeleon, or Cary WinUV.
• Strong attention to detail and the ability to manage priorities independently.
• Bachelor’s degree in chemistry, biochemistry, or a related scientific field preferred; equivalent relevant experience will be considered.

Equal Opportunity Employer

Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, age (40 and over), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. Jobot also prohibits harassment of applicants or employees based on any of these protected categories. It is Jobot’s policy to comply with all applicable federal, state and local laws respecting consideration of unemployment status in making hiring decisions.

Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.