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Quality Control In-Process Analyst

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Onsite

Quality Control In-Process Analyst

BioTalent

Quality Control In-Process Analyst

Skills

Compliance

3 days ago

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Important information


Contract type:

Permanent

Salary:

$25 – $32 / hour

Location:

Tustin, CA, USA

Work mode:

Onsite

Published on:

19 October 2026

What they need


Quality Control In-Process Analyst

Location: Tustin, CA

About the Role

We are partnering with a leading biopharmaceutical manufacturing organization seeking a Quality Control In-Process Analyst to support manufacturing, validation, process development, and stability studies within a GMP-regulated environment. This role is responsible for performing analytical testing, sample collection, data analysis, and documentation activities that ensure product quality and compliance throughout the manufacturing process.

Key Responsibilities

  • Perform analytical and compendial testing in accordance with established protocols and GMP requirements.
  • Analyze test data, document results, and prepare reports with a high degree of accuracy.
  • Conduct aseptic sampling and in-process testing, including pH, conductivity, osmolality, A280, endotoxin (LAL), and other quality control assays.
  • Prepare buffers, reagents, and testing materials needed for laboratory operations.
  • Perform water testing and raw material sampling and testing activities.
  • Perform QC testing for lot release, stability, development/validation projects, and investigations.
  • Write and revise test methods, standard operating procedures (SOPs), study protocols, and technical reports.
  • Collaborate with cross-functional teams to develop, improve, and implement quality control procedures and policies.
  • Ensure compliance with current Good Manufacturing Practices (cGMP), laboratory procedures, and applicable regulatory requirements.

Qualifications & Requirements

  • B.S. degree in Biology, Chemistry, Biomedical Engineering, Chemical Engineering, or a related scientific discipline.
  • 2+ years of experience in a biotechnology, pharmaceutical, or GMP-regulated laboratory setting.
  • Must have experience with analytical testing, writing reports, GMPs, and regulatory audits.

This position is not eligible for visa sponsorship or support such as H1B, TN, E-3, CPT, OPT, STEM OPT, or employment-based permanent residence processes, now or in the future.

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