Quality Control Analyst III – Biotech, cGMP

AppleOne Employment Services

Camarillo (CA)

On-site

USD 116,000 - 175,000

Full time

11 days ago

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Job summary

AppleOne Employment Services in Camarillo, CA seeks a Quality Control Analyst III to join a regulated biotech/pharma lab. You will perform complex analytical testing (HPLC, ELISA), evaluate data, and support investigations, CAPAs, and stability programs in a cGMP/GLP environment.

The role offers collaboration across functions, opportunities to drive process improvements, and mentoring of junior staff while maintaining strict quality and compliance standards in a fast-paced lab setting.

Qualifications

  • Experience performing complex analytical testing in a regulated environment.
  • Familiarity with HPLC, ELISA, and related QC techniques.
  • Strong data evaluation skills and trend analysis.
  • Experience supporting investigations, change controls, and CAPA.

Responsibilities

  • Perform complex analytical testing and data evaluation using methods such as HPLC, ELISA, and other QC laboratory techniques.
  • Troubleshoot laboratory equipment issues, support equipment upkeep, and communicate resolutions to management.
  • Support method validations, SOP revisions, protocols, reports, investigations, change controls, and data summaries.
  • Investigate OOS events, perform root cause analysis, assess product impact, and support CAPA implementation.
  • Coordinate testing with outside laboratories and cross-functional departments, including raw material testing and scheduling priorities.
  • Lead stability program activities, including test point management, data reporting, trend evaluation, and investigation of aberrant results.

Skills

Analytical testing
HPLC
ELISA
Data evaluation
cGMP/GLP
Investigations

Job description

AppleOne Employment Services in Camarillo, CA seeks a Quality Control Analyst III to join a regulated biotech/pharma lab. You will perform complex analytical testing (HPLC, ELISA), evaluate data, and support investigations, CAPAs, and stability programs in a cGMP/GLP environment.

The role offers collaboration across functions, opportunities to drive process improvements, and mentoring of junior staff while maintaining strict quality and compliance standards in a fast-paced lab setting.

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