JT
Staff Engineer I, THV Research and Development-THV
Accepting applicationsJenaValve Technology, Inc. · Irvine, CA
Full-Time Senior
Posted
2d ago
Category
Manufacturing
Experience
Senior
Country
United States
Job Title: Staff Engineer, THV Research and Development
Staff Engineer I, Research and Development
Staff Engineer II, Research and Development
Staff Engineer III, Research and Development
Supervisor/Manager Title: Director, Research and Development
Job Description Summary: Responsible for the development of novel subsystems and components for transcatheter heart valves and/or delivery systems.
Job Responsibilities
Conceive, design, and develop components and subsystems of moderate/high complexity for transcatheter heart valves and/or delivery systems in accordance with quality system requirements and with minimal supervision.
Create, review and/or approve component and subsystem drawings/specifications and documentation.
Identify/evaluate vendors, procure components and develop component specifications.
Develop test methods, conduct testing, and interpret data.
Conduct engineering analyses and feasibility testing of components and subsystems to ensure proper fit and function.
Conduct competitive product evaluation and product failure analyses.
Partner with Quality to conduct risk analyses and develop/execute design verification activities.
Partner with Manufacturing to develop manufacturing processes, tooling/fixtures, and transfer product/processes to manufacturing.
Supervise R&D Technicians.
Qualifications
Required Education and Experience:
A Bachelor of Science degree in Engineering or Technical discipline with related work experience.
Minimum of 6+ years’ experience in R&D or product development of medical devices, pharmaceutical or life science product technology. Level I, II, III DOE
Familiarity with 21CFR820 and ISO 13485 requirements.
Knowledge of the product development process and applicable Quality System requirements in the medical device industry.
Demonstration of ability to work effectively and collaborate within cross-functional teams.
Demonstration of ability to effectively communicate (in oral presentation and written documentation) test protocols, reports, and technical summaries to technical and non-technical personnel.
Hands-on experience in product development within an R&D lab environment.
Skills And Abilities Required For This Job
Ability to work independently and in collaboration within cross-functional teams.
Ability to manage multiple tasks in a timely manner with high attention to detail.
Ability to build strong relationships at all levels of the organization, cross-functionally and with key external personnel.
Demonstrated strength in problem analysis, judgment, decision making and critical thinking
Strong written and verbal communication.
Experience in developing product specifications based on user needs and writing design verification and validation protocols.
Strong Solidworks/CAD skills.
Project management skills.
Knowledge of statistical analysis and applications.
Show more Show less
Staff Engineer I, Research and Development
Staff Engineer II, Research and Development
Staff Engineer III, Research and Development
Supervisor/Manager Title: Director, Research and Development
Job Description Summary: Responsible for the development of novel subsystems and components for transcatheter heart valves and/or delivery systems.
Job Responsibilities
Conceive, design, and develop components and subsystems of moderate/high complexity for transcatheter heart valves and/or delivery systems in accordance with quality system requirements and with minimal supervision.
Create, review and/or approve component and subsystem drawings/specifications and documentation.
Identify/evaluate vendors, procure components and develop component specifications.
Develop test methods, conduct testing, and interpret data.
Conduct engineering analyses and feasibility testing of components and subsystems to ensure proper fit and function.
Conduct competitive product evaluation and product failure analyses.
Partner with Quality to conduct risk analyses and develop/execute design verification activities.
Partner with Manufacturing to develop manufacturing processes, tooling/fixtures, and transfer product/processes to manufacturing.
Supervise R&D Technicians.
Qualifications
Required Education and Experience:
A Bachelor of Science degree in Engineering or Technical discipline with related work experience.
Minimum of 6+ years’ experience in R&D or product development of medical devices, pharmaceutical or life science product technology. Level I, II, III DOE
Familiarity with 21CFR820 and ISO 13485 requirements.
Knowledge of the product development process and applicable Quality System requirements in the medical device industry.
Demonstration of ability to work effectively and collaborate within cross-functional teams.
Demonstration of ability to effectively communicate (in oral presentation and written documentation) test protocols, reports, and technical summaries to technical and non-technical personnel.
Hands-on experience in product development within an R&D lab environment.
Skills And Abilities Required For This Job
Ability to work independently and in collaboration within cross-functional teams.
Ability to manage multiple tasks in a timely manner with high attention to detail.
Ability to build strong relationships at all levels of the organization, cross-functionally and with key external personnel.
Demonstrated strength in problem analysis, judgment, decision making and critical thinking
Strong written and verbal communication.
Experience in developing product specifications based on user needs and writing design verification and validation protocols.
Strong Solidworks/CAD skills.
Project management skills.
Knowledge of statistical analysis and applications.
Show more Show less