About this opportunity
imperativecare lists this Sr Clinical Engineer opportunity in campbell, California. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Title: Sr Clinical Engineer
This position is based in our Campbell, California offices. This position is on-site and full time.
Why Imperative Care?
Do you want to make a real impact on patients? As part of our team at Imperative Care, you can help elevate care for patients suffering from stroke and other devastating vascular diseases. Every day, the technologies that we develop at Imperative Care directly impact people at the most vulnerable moments of their lives. Our focus is on the needs of the patient, and they come first in everything we do.
What You’ll Do
As a seasoned professional in this field, the Sr Clinical Engineer is responsible for gathering clinical or user data to inform the definition, specification, design and testing of pre-commercial and commercial vascular and/or stroke products, with heavy emphasis on our stroke portfolio. This team member will interact directly with clinical customers as well as with cross functional internal teams. They must possess significant initiative and be intellectually disposed toward exploring and making sense of the unknown and lead the support of pre-clinical testing, training and support in clinical procedures for internal and external stakeholders using the product(s).
Serve as a clinical engineering team member for product development including preclinical testing, bench testing, model development needs, in-vitro test methods and plans and in-vivo animal studies.
Provide updates to team members and management (as needed) regarding project status, and critical issues that may affect attainment of project completion dates.
Create and execute design verification and testing plans, participating in team meetings where progress is discussed, decisions are made, and updates are communicated.
Ensure work effort supports pre-clinical testing of new products within the design control and applicable quality standards, and products are designed, developed, tested, manufactured and documented according to applicable global regulatory requirements.
Support new team members or interns though product and procedure training as needed
Ensure detailed plans are executed fully to support internal development projects with preclinical testing including bench testing, model development needs, in-vitro test methods and plans and in-vivo animal studies.
Interact directly with clinical customers to identify customer input requirements for the system
Plan and conduct ethnography studies
Interact directly with commercial and marketing partners to identify gaps and potential solutions to existing customer needs
Provide inputs to help quantify performance requirements for our products
Work with design engineers to translate customer input requirements to design input requirements
Drive completion of pre-clinical testing including validation testing
Develop test models
Create test plans, protocols, reports for all testing ensuring all documentation is aligned to company procedures and QMS
Responsible for planning, conducting and completing lab activities including maintaining inventory, ordering materials, setting up and keeping lab areas clean
Handle complaints and market claims as requested
Support commercial events such as conferences by providing product demos or physician engagements
What You’ll Bring
BS in Engineering or related discipline or equivalent and 5+ years of experience with increasing responsibility in novel product or procedure development in the medical device industry or equivalent combination of education and experience
Experience in one of the following fields: vascular/neurovascular interventions or surgical robotics
Demonstrated ability to take initiative to start projects, create and meet deadlines.
Demonstrated success working with cross functional teams and customers (physicians and hospital staff)
Previous involvement in at least one full product development cycle
Knowledge of and exposure to product testing and data collection
Experience working under quality systems designed to meet governmental regulations such as FDA QSR, ISO 13485 and the MDD
Strong working knowledge of relevant regulatory standards that apply to the specific product/project
Familiarity with Design control procedures and requirements
Excellent communication skills (both written and verbal)
Ability to work independently or in a team setting required and ability to travel as required for the role;
Employee Benefits
include a stake in our collective success with stock options, competitive salaries, a 401k plan, health benefits, generous PTO, and a parental leave program.
Join Us!
Imperative Care
Salary Range: $140,000 – 150,000 annually
Please note that the salary information is a general guideline only. Imperative Care considers factors such as scope and responsibilities of the position, candidate's work experience, education/training, key skills, and internal equity, as well as location, market and business considerations when extending an offer. As part of our total rewards package, Imperative Care offers comprehensive benefits including a 401k plan, health benefits, generous PTO, a parental leave program and emotional health resources.
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Worksite address
campbell, CA, 95011, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.