Analytical QC Scientist II: In-Process & Release Testing

Valid8 Financial, Inc.

Florida

On-site

USD 65,000 - 90,000

Full time

2 days ago
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Job summary

Valid8 Financial, Inc. is seeking an Analytical Quality Control Associate II to perform routine in-process, release, and stability testing for drug substance and product samples.

You will support method qualification and transfer activities, collaborate with cross-functional teams, and handle documentation under general supervision. The role requires 2–4 years of QC testing in a cGMP/GLP setting, with experience in HPLC/UPLC, CE-SDS, qPCR, ELISA, and related techniques.

Qualifications

  • Bachelor's degree in Chemistry, Biochemistry, Biology, or a related scientific discipline.
  • 2–4 years of analytical QC testing in a cGMP/GLP environment preferred.
  • Experience with core analytical techniques (HPLC/UPLC, CE, UV-Vis, molecular assays).

Responsibilities

  • Perform routine in-process, release, and stability testing on samples.
  • Support method qualification, validation, and transfer activities.
  • Analyze data and peer-review laboratory testing data and notebooks.
  • Draft and revise SOPs, test methods, and CoAs.
  • Initiate investigations, CAPAs, and deviations under supervision.
  • Maintain instrument readiness and GMP logbooks; manage supplies.
  • Coordinate sample shipments and timelines with external labs.
  • Assist audits and regulatory inspections with documentation.

Skills

Analytical QC testing
Data analysis
Documentation

Education

Bachelor's degree in Chemistry, Biochemistry, Biology, or related

Tools

Empower
ChemStation
LIMS
MS Office

Job description

Valid8 Financial, Inc. is seeking an Analytical Quality Control Associate II to perform routine in-process, release, and stability testing for drug substance and product samples.

You will support method qualification and transfer activities, collaborate with cross-functional teams, and handle documentation under general supervision. The role requires 2–4 years of QC testing in a cGMP/GLP setting, with experience in HPLC/UPLC, CE-SDS, qPCR, ELISA, and related techniques.

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