QC Data Reviewer

Costa Mesa, CA, US • Posted 19 hours ago • Updated 50 minutes ago
Contract W2
On-site
USD $32.00 - 40.00 per hour
Fitment

Dice Job Match Score™

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Job Details

Skills

  • Contract Management
  • Process Engineering
  • Life Sciences
  • Procurement
  • Vendor Management
  • Inventory
  • Leadership
  • Business Development
  • Project Management
  • Supply Chain Management
  • Accountability
  • Collaboration
  • Continuous Improvement
  • Analytical Chemistry
  • Regulatory Compliance
  • Manufacturing
  • Auditing
  • Test Methods
  • Pharmaceutics
  • Biotechnology
  • Quality Control
  • Data Quality
  • GMP
  • Good Manufacturing Practice
  • Documentation
  • Data Integrity
  • Analytical Skill
  • HPLC
  • UV
  • TOC
  • Theory Of Constraints
  • Testing
  • Attention To Detail
  • Management
  • Chemistry
  • Biochemistry
  • Military
  • SAP BASIS
  • Authorization
  • Law
  • LOS
  • Recruiting
  • Legal
  • Artificial Intelligence
  • Privacy

Summary

This Jobot Consulting Job is hosted by: Christian Aviles
Are you a fit? Easy Apply now by clicking the "Apply Now" 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 "Apply Now" button.

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  • Dice Id: 91113390
  • Position Id: 483518848
  • Posted 19 hours ago
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