Cordis · 5 months ago
Staff Engineer Research and Development (Onsite)
Santa Clara, California
Full-time
Onsite
Lead/Staff
8+ years expCordis is a global leader dedicated to transforming cardiovascular care and saving lives through innovative technology. The Staff Engineer in Research and Development will focus on designing and developing vascular closure devices, ensuring compliance with regulations, and leading engineering projects with significant organizational impact.
Health CareHealth DiagnosticsMedical
Responsibilities
Applies comprehensive medical device engineering knowledge and a thorough understanding of concepts, principles, and technical capabilities to achieve design realization of medical devices
Plans and develops engineering projects concerned with unique or controversial problems which have an important effect on major organization programs. This involves exploration of subject area, definition of scope and selection of problems for investigation and development of novel concepts and approaches
Identifies internal and external customer needs. Translates needs and requirements into tests cases for design verification and validation
Accountable for design reviews as applicable ensuring that verification and validation tests are documented, evaluated against design input, and executed properly
Develops and monitors work schedule to ensure on time completion of testing activities assigned
Supervision received is essentially administrative with assignments given in terms of broad general objectives and limits
Acts as individual technical expert, conceives or is assigned, plans, and conducts research in problem areas of considerable scope and complexity
Anticipates, plans, and implements new innovative test methods; provides critical design input to specific situations; has a broader knowledge of the testing environment; gains cross functional alignment across the organization
Able to summarize results of design work and research studies concisely. Participates in the regulatory submission process as a subject matter expert. Supports regulatory by providing technical justifications for submissions, reviewing regulatory filings, and answering technical questions during planned meetings
Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental
Qualification
Required
Bachelor's degree in Mechanical Engineering or Biomedical Engineering is required
A minimum of 8 years related work experience and design experience in vascular closure device preferred
Proven ability in the design and development (including process engineering) of cardiovascular catheter technologies including design experience in vascular closure devices
Must possess clearly recognizable outstanding technical qualifications and leadership
English communication skills, written and oral
Preferred
MS Degree in Engineering discipline preferred
Proven proficiency in Computer Aided Design or SolidWorks preferred
Company
Cordis
Cordis Corporation, a Johnson & Johnson company, has pioneered less invasive treatments for vascular disease.
1001-5000 employees
H1B Sponsorship
Cordis has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (5)
2024 (3)
2023 (3)
2022 (4)
Funding
Current Stage
Late StageTotal Funding
unknown2021-03-12Acquired
Leadership Team
Scott Drake
Chief Executive Officer
Recent News
2025-11-11
TeamBest Global Companies
2025-11-07
News-Medical.Net
2025-11-01
Company data provided by crunchbase