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Principal Systems Engineer (dublin / pleasanton / livermore)
By | July 27, 2007
As the pioneers of Polymerase Chain Reaction (PCR) technology, Roche Molecular Diagnostics has embarked on an incredible adventure that has not only launched the use of reliable DNA-based tests into laboratories worldwide, but has also aided the genetics revolution, which is dramatically altering the future of medical care. Every day is a new opportunity to create novel diagnostic tools, close the gap on infection and detection, and take the power of genomics to the next level to identify potential diseases before they occur. ItÂ’s an exciting place to be, and the journey has just begun. We currently seek an experienced professional to join our Pleasanton, CA facility.
Principal Systems Engineer
The Systems Development department is in need of a very knowledgeable and experienced Scientist/Engineer with a background in medical device design, development, validation and product support. The successful candidate will work as part of a Systems Development sub-team focusing on development, validation and support of the cobsa s 401 and/or the cobas s 201 Blood Screening System(s). Candidate will interface with hardware and software developers, will work closely with internal reagent development teams, and will work with Roche Global Systems Support during product field testing and commercialization. Involves designing and conducting feasibility tests and experiments to integrate and evaluate reagents, hardware and software towards assessing feasibility of complete automated test systems for IVD and Blood Screening applications, in addition to working with a team in designing and writing technical reports, test plans, validation test protocols/reports and risk assessments.
Requires a Master’s degree in Chemistry, Engineering, Biological/Life Science or a related field; 5-10 years of relevant instrument, hardware and/or software development experience; and 5-10 years experience in the medical device industry, within project and technical leadership roles. Must have experience in medical device development processes and methodologies across multiple disciplines and subject matters. Experience with FDA-regulated system development/design control and technical product support is desired.
For more info and for consideration, please visit our website and apply online, indicating Job Code RMD070143 at: http://careers.ind.roche.com/joblist.html. Principals only, please. We are committed to providing equal opportunity to a diverse workforce.
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