SYSTEMS ENGINEER I 11.4.9 updated
Adecco Technical & Scientific, a division of the world leader in the recruitment of Technical and Scientific professionals, has an immediate opening for a SYSTEM ENGINEER on a CONTRACT opportunity in Tri-Valley Area.
SYSTEM ENGINEER I. The candidate will be knowledgeable and experienced scientist/engineer preferable with background in software testing, medical devices, development and validation. It is desired that the candidate have experience with troubleshooting the system. Understanding of medical device development processes and methodologies across multiple disciplines and subject matters (medical device design control, development/ operation of diagnostic instrumentation, system and software validation testing, documentation) is preferred. The candidate will work as part of Systems Development sub-teams, and will participate on cross-functional project teams. The candidate may interface with external hardware and software developers, and will work closely with internal reagent development teams. Candidate should have extended knowledge of the technology associated with PCR RT-PCR, DNA, CLONING, etc. Experience with FDA regulated system development/design control is desired, and ability to manage his/her own work independently is required
Duties will include:
-Participate in installation of software, networking computers, testing of software beta versions, troubleshooting, and validation testing. Prepare appropriate technical documentation for product design history files and FDA submissions.
-Assist in customer (internal and external) support issues, such as installation, troubleshooting, and follow-up, as required.
-Work with team in ad hoc testing of software as well as manage the analysis, reporting, and documentation of test results and new and existing software and system elements against requirements.
-Plan, manage and execute assigned development-related laboratory experiments/projects utilizing established and/or innovative procedures, applying scientific knowledge and accumulated experience to complete projects.
-Work with technical teams to create, develop, and execute validation test cases and compile associated documentation. Apply advanced technical writing skills to produce reports and documents.
-Analyze date, evaluation results, form conclusions, and provide and/or implement product, process, or document improvements.
-Ensure activities are consistent with project critical path, and respond appropriately to changing priorities.
-Present findings at group meetings, as required
Requirements:
BS Degree in Biological/Life Science, Chemistry, Computer Science or related field, or equivalent combination of education and work-related experience .
Minimum 2 to 3 years relevant hardware and/or software development experience or equivalent combination of education and/or work related experience.
Experience in trouble-shooting is a plus.
Experience in medical device industry preferred, but not required.
Experience with software testing and/or software development.
Experience working with cross-functional teams/individuals.
Drug/Background check will be required.
If you are interested in this opportunity email james.ratliff@adeccona.com or call 925-686-8422 Ext. 14.
Adecco Group is a Fortune Global 500 company and the global leader in HR services. Our group connects over 700,000 associates with our business clients each day through our 6,600 offices in over 70 countries and territories around the world. We offer employment opportunities at any stage in your professional career. Contact us today to discuss available contract and direct hire positions. www.AdeccoUSA.com