DNA Script
DNA Script is a leading company in the production of nucleic acids for genomic, synthetic biology and biopharmaceutical applications.
Our clean, efficient Enzymatic DNA Synthesis (EDS) technology, implemented on a benchtop instrument (the SYNTAX), accelerates innovation in life science and biotechnology through the decentralization of rapid, on demand and high quality DNA synthesis.
Our approach builds upon nature's billions of years of evolution in enzymatically synthesizing DNA, setting new standards for assembling nucleic acids to accelerate scientific discovery and DNA/RNA production in disciplines with profound impacts upon humanity.
DNA Script has a broad stable of high quality investors and is capitalized to continue its progress to full commercialization of the technology and products. We are building an organization across our two sites, in Paris and San Francisco, with the talent, skills and attitude to achieve our mission: to unlock the power of "DNA-write".
This is an opportunity for a dynamic individual to join an international and highly skilled team, and to make significant contributions to commercializing a technology with far-reaching potential across the biological sciences and beyond.
Must have at least 1 year of prior work experience in each of the following:
1. Verification and validation experience in one of the following regulated industries: in vitro diagnostics, medical device, or biotech
2. Systems verification and validation principles while working in biotech, pharma industry, or clinical research
3. Develop, author and review system specifications, risk assessments, plan, protocols, and reports as they relate to the system and intended use to evaluate product requirements
4. Development and execution of test method validations, installation and qualification of systems, and Computer Systems Validation
5. Identifying and remediating issues found during testing