Bioanalytical Research Associate II - GLP/Non-GLP

Zenith LifeScience LLC.

South San Francisco (CA)

On-site

USD 85,000 - 135,000

Full time

32 hours ago
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Job summary

Zenith LifeScience LLC. is seeking a Research Associate II to support and execute nonclinical bioanalytical activities in GLP and non-GLP environments. You will handle sample processing, assay execution, data analysis, documentation, and training of other analysts.

Responsibilities include extracting nucleic acids from tissue, running ddPCR/qPCR/ELISA/MSD, and ensuring compliant SOPs and GDP documentation. Collaboration with teams to generate high-quality data is expected.

Qualifications

  • BS in Biology or related field (MS preferred).
  • Hands-on experience qPCR/ddPCR, ELISA or MSD.
  • 5+ years of hands-on experience in a bioanalytical, molecular biology or related laboratory setting.
  • Experience following SOPs and study documentation.
  • Good Documentation Practices (GDP) experience.
  • Strong communication and organizational skills.

Responsibilities

  • Nonclinical bioanalytical activities in GLP and non-GLP environment.
  • Extract protein, DNA, and/or RNA from necropsied animal tissue.
  • Run ddPCR, qPCR, ELISA, MSD, Western blot, and related analyses on tissue extracts.
  • Perform nonclinical sample analysis.
  • Support drafting and maintenance of analysis plans and SOPs.
  • Data analysis, compilation, and QC.
  • Train and support other analysts on bioanalytical methods, workflows, and best laboratory practices.

Skills

qPCR/ddPCR
ELISA
Molecular biology
Data analysis

Education

BS in Biology
MS preferred

Tools

LIMS/ELN
GraphPad Prism
Excel
SnapGene

Job description

Zenith LifeScience LLC. is seeking a Research Associate II to support and execute nonclinical bioanalytical activities in GLP and non-GLP environments. You will handle sample processing, assay execution, data analysis, documentation, and training of other analysts.

Responsibilities include extracting nucleic acids from tissue, running ddPCR/qPCR/ELISA/MSD, and ensuring compliant SOPs and GDP documentation. Collaboration with teams to generate high-quality data is expected.

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