We are looking for a System Engineer I, working in the Healthcare Systems & Services industry in Santa Clara, California, United States.
Organizes, conducts, and monitors laboratory experiments utilizing established and published procedures, building technical and theoretical understanding.
Assumes responsibility for the accuracy, quality, and timeliness of experimental results.
Works with cross-functional teams to contribute to Risk and Requirements Management processes under design control procedures.
Exercises creative, imaginative thinking when required to resolve complex issues.
Makes recommendations to resolve issues encountered during experimental procedures.
Communicates results to supervisor and/or team via written reports and oral presentations.
Assesses results for applicability, validity, and conformance to Product Requirements.
Performs work according to established internal safety guidelines and procedures, and as specified by appropriate external regulatory agencies (e.g. OSHA).
The pay range we are offering is 30 to 40 per hour. This position may present an opportunity to go permanent.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
Bachelors in engineering, sciences, or related field required
0-3 years relevant industry experience; MS with fewer years of work experience may be acceptable
Experience with experimental design, laboratory practice, data analysis, and data and concept presentation required
Experience with all phases of technology development is desirable
Experience in RUO or IVD product design and development is desirable
Specific experience in Requirements Management as well as the Design Verification process for biomedical systems is highly desirable
Knowledge of Risk Analysis methods, Reliability Engineering, or Design Transfer activities for product manufacturing is desirable
Nucleic acid based technology background and next-generation sequencing experience are highly desirable
Other system development experience in complex diagnostic development environments is a plus
Knowledge of NGS workflows and data analysis is desirable. Experience with NGS systems development is a plus
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.