- Looking for local candidates to be onsite daily in Pleasanton.
- Travel to Santa Clara 5% on an as needed basis.
- After introduction to work processes, begins to organize, conduct and monitor laboratory experiments utilizing established and published procedures, and technical and theoretical understanding. Assumes responsibility for the accuracy, quality, and timeliness of experimental results. Summarizes experimental results, and reviews conclusions with supervisors/project leader. Communicates results of experiments. Keeps supervisor/project leader informed of project status, particularly of significant findings and results in critical problem areas. Performs work according to established internal safety guidelines and procedures, and as specified by appropriate external regulatory agencies (e.g., OSHA).
Evaluates new equipment and techniques.
Selects techniques to solve problems and makes sound design recommendations.
Assesses results for applicability, validity, and conformance to Product Requirements.
With guidance, analyzes and brainstorms alternative approaches to solve problems and find solutions.
May coordinate work of technologists & technicians and other support personnel, as needed within the project context.
Work is typically routine/standard in nature; non-routine situations may arise, but are typically limited in complexity and frequency.
Other duties as assigned by management.
Minimum Qualifications:
0-3 years of industry experience.
Preferred - Medical device experience.
REQUIRED - Bio-medical engineering or bio-engineering BA degree.
Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
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