QC Data Reviewer

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This Jobot Consulting Job is hosted by: Christian Aviles
Are you a fit? Easy Apply now by clicking the "Quick Apply" button and sending us your resume.
Salary: $32 - $40 per hour

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.

Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.

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