Offer summary
Qualifications:
PhD in Nucleic Acids Biochemistry, Molecular Biology, or related field, MS with 2 years relevant experience in NGS assay development, BS with 4-8 years relevant industry experience, Experience in CAP/CLIA regulated environments, Hands-on knowledge of nucleic acid technologies like NGS and PCR.
Key responsabilities:
- Lead transfer and validation of molecular diagnostic assays
- Prepare clinical sample artifacts for validation studies
- Manage validation planning and reporting documents
- Train clinical staff on assay operation
- Document performance specifications and troubleshoot issues