Specialist/Senior Specialist, Quality Control Analytical

COMPANY:

Clinical and preclinical stages of development for genomic medicines for serious diseases (gene & cell therapy & genome editing)

LOCATION:

Greater San Francisco area

TITLE:

Specialist/Senior Specialist, Quality Control Analytical - full-time, permanent

**Must have cell or gene therapy experience to be considered**

RELOCATION ASSISTANCE:

Some assistance available

ROLE RESPONSIBILITIES:

This individual will perform QC activities associated with the cGMP production and release testing of the company's products. This person will also be responsible for routine analytical chemistry and cell-based assays testing and review, QC SOPs initiation and revision, lab setup and maintenance, QC method validation and transfer activities.

CANDIDATE REQUIREMENTS:

• A minimum BS degree in a relevant, scientific field + 2-5 years of QC working experience in analytical lab settings in the pharma or biologics industry
• Hands-on experience in the in-process product testing and release activities
• Must have hands-on experience with analytical instrumentation such as pH meter, Osmometer, UV spectrophotometer, HPLC, etc.
• Strong hands-on knowledge associate with cell or gene therapy analytical assays (qPCR, ddPCR, flow cytometry, ELISA)
• Technical knowledge in ddPCR, ELISA, flow cytometry assay and some cell-based assays

If you meet the requirements above and would like to be considered for this position, apply on-line now for immediate consideration and to be contacted with further details.