This position will play a pivotal role within the Ion Torrent clinical product development. The unique individual selected for this position will have high visibility throughout the company. Responsibilities include interacting with cross-functional teams from R&D, operations, quality, and regulatory affairs. If you have experience in DNA sequencing and developing assays in the in vitro diagnostics industry, this could be a very exciting position for you.
- Will develop and validate an automated next generation IVD sequencing system based on Ion Torrent technology with the objective of meeting FDA regulatory requirements for commercialization.
- You will apply your management and laboratory skills and experience working in the regulatory environment for IVD product development, verification and validation, manufacturing and transfer, and commercialization.
- The ability to communicate with stakeholders, manage projects, meticulously document and communicate results to diverse audiences is important aspects of this role.