Discover Your Role
- Plan, initiate, and execute qPCR, digital droplet PCR (ddPCR), and ELISA assays.
- Prepare samples and perform assay runs supporting preclinical and clinical programs.
- Process assay data and maintain compliance with current GxP documentation.
- Document findings and laboratory records in an electronic laboratory notebook.
- Evaluate new technologies and assay formats to advance development capabilities.
- Maintain Good Laboratory Practice (GLP) compliance for validations under FDA regulations and SOPs.
- Present scientific data in formal and informal meetings.
- Collaborate cross-functionally and take ownership of deliverables.
This Role Requires
- Bachelorβs degree in biology or a related field; Masterβs degree preferred.
- 3 to 6+ years of relevant laboratory experience.
- Hands-on experience with qPCR and ddPCR.
- Understanding of DNA/RNA assessment methodologies.
- Experience with biochemical, molecular, and immune-based assays, including ELISA.
- Ability to manage multiple assays/projects simultaneously.
- Experience with GxP documentation and GLP-compliant laboratory records.
- Experience with electronic laboratory notebooks.
- Gene therapy and/or bioanalytical assay platform development experience highly desirable.
- Strong problem-solving, prioritization, communication, organization; ability to work independently.