Home › Companies › Imperativecare › Sr R&D Engineer
Sr R&D Engineer
Imperativecare · Campbell, CA, 95008 · Active · $132,000 / year · JazzHR / ApplyToJob
Job facts
| Field | Value |
|---|---|
| Company | Imperativecare |
| Title | Sr R&D Engineer |
| Normalized title | - |
| Department / team | - |
| Location | Campbell, CA, United States |
| Work model | - |
| Employment type | Full Time |
| Salary | $132,000 / year |
| Status | active |
| ATS provider | JazzHR / ApplyToJob |
| Posted / first seen | 2026-04-21 / 2026-05-30 |
| Changed / last seen | 2026-05-30 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Imperativecare. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through JazzHR / ApplyToJob. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Campbell. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Imperativecare |
| Source | cade5286-aa33-4e90-940f-d7a3fd45cd44 |
| ATS provider | JazzHR / ApplyToJob |
Description
Job Title: Sr R&D Engineer
Location : This position is based in our Campbell, California offices. This position is full time.
Why Imperative Care?
Do you want to make a real impact on patients? Imperative Care is changing the way stroke is treated. As part of our team, you’d be developing breakthroughs that will revolutionize the future of stroke care. Every day, the technologies that we develop at Imperative Care directly impact human lives. Our focus is on the needs of the patient, and they come first in everything we do.
What You’ll Do
As a senior professional, this position will use solid knowledge and experience to design, develop and launch innovative endovascular/neurovascular products through conceptualization, design development, verification/validation, and manufacturability assessments. This role will deliver ideation and prototyping, establishing requirements/specifications and verification of performance inputs and outputs. Serve as technical team member or lead in project transfers from early-stage teams into formal design control programs, executing projects based on value improvement, line extensions, and compliance on commercialized products. Respond to technical field inquiries and perform root-cause investigations on product failures. Create, modify, and qualify test methods per FDA and regulatory requirements. Establish and/or tune detailed requirements including product specifications and appropriate test methods through activities such as competitive testing, literature review and KOL engagement. Author robust component/assembly drawings, specification documents, test protocols and reports. Ensure technical activities are properly documented; participate in and contribute to technical discussion sessions to generate new intellectual property.
What You’ll Bring Bachelor’s degree in engineering, or related discipline and a minimum of 5 years of related experience in the medical device or related regulated industry; or equivalent combination of education and work experience. Experience in endovascular or neurovascular techniques and devices preferred. Statistical Analysis Software (Minitab or similar) and CAD (Solidworks, ProE, similar). Skilled knowledge of machine shop equipment (mill, lathe, drill press, etc.) operation including operation of 3D printing equipment is preferred. Developing knowledge of product design from concept to regulatory marketing approval. Ability to complete projects individually as well as part of a team, exercising judgment within defined procedures and practices to determine appropriate action. Ability to apply learned techniques to analysis/investigation to solve challenges using problem-solving tools and methodologies. Previous experience working with regulated quality systems such as GMPs, ISO 9001, and the MDD. Familiar with Design Control procedures and requirements.
Employee Benefits include a stake in our collective success with stock options, bonus, competitive salaries, a 401k plan, health benefits, generous PTO, and a parental leave program.
Join Us! Apply Today .
Salary Range: $132,000 - 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.
The use of external recruiters/staffing agencies requires prior approval from our Human Resources Department. The Human Resources Department at Imperative Care requests that external recruiters/staffing agencies not to contact Imperative Care employees directly in an attempt to present candidates. Complying with this request will be a factor in determining future professional relationships with Imperative Care.
Imperative Care will not accept unsolicited resumes from any source other than candidates themselves for either current or future positions. Submission of unsolicited resumes in advance of an agreement between the Human Resources Department and the external recruiter/staffing agency does not create any implied obligation on the part of Imperative Care.
Full job record
| Job ID | b3c2eefdf7d4cc8d0ff51591f9fc42cf2cb4a221 |
| Org ID | b2419ccb-c14b-43dc-b827-465290ac8fd3 |
| Source ID | cade5286-aa33-4e90-940f-d7a3fd45cd44 |
| Board ID | cade5286-aa33-4e90-940f-d7a3fd45cd44 |
| Provider | jazzhr |
| Provider Job Key | k4RwubZAks |
| Title | Sr R&D Engineer |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Campbell, CA, 95008 |
| Department | — |
| Team | — |
| Employment Type | full_time |
| Workplace Type | — |
| Remote Policy | — |
| Country | United States |
| Region | CA |
| City | Campbell |
| Salary Raw | Salary Range: $132,000 - 150,000/annually Please note that the salary information is a general guideli |
| Salary Min | 132,000 |
| Salary Max | — |
| Salary Currency | USD |
| Salary Period | year |
| Source URL | https://imperativecare.applytojob.com/apply/k4RwubZAks/Sr-RD-Engineer |
| Apply URL | https://imperativecare.applytojob.com/apply/k4RwubZAks/Sr-RD-Engineer |
| First Seen At | 2026-05-30 06:05:28Z |
| Last Seen At | 2026-06-06 10:50:38Z |
| Last Checked At | 2026-06-06 10:50:38Z |
| Last Changed At | 2026-05-30 06:05:28Z |
| Inactive At | — |
| Source Posted At | 2026-04-21 00:00:00Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=jazzhr/board=imperativecare/date=2026-06-06/2026-06-06T10-50-36-289Z-9978bb13ad458de8b79e52f4b96ce7232e5c5cb1515c2a8c446a530dda7413c5.json |
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"description_html": "<span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-size:12pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Job Title: Sr R&D Engineer </span></span></span></b></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-family:Roboto;\">Location</span></b><i><span style=\"font-family:Roboto;\">: This position is based in our Campbell, California offices. This position is <u>full time.</u></span></i></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-family:Roboto;\"><span style=\"color:#ed7d31;\">Why Imperative Care?</span></span></b></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"font-family:Roboto;\">Do you want to make a real impact on patients? Imperative Care is changing the way stroke is treated. As part of our team, you’d be developing breakthroughs that will revolutionize the future of stroke care. Every day, the technologies that we develop at Imperative Care directly impact human lives. Our focus is on the needs of the patient, and they come first in everything we do.</span></span></span></span><br><br><span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-family:Roboto;\"><span style=\"color:#ed7d31;\">What You’ll Do</span></span></b></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"font-family:Roboto;\">As a senior professional, this position will use solid knowledge and experience to design, develop and launch innovative endovascular/neurovascular products through conceptualization, design development, verification/validation, and manufacturability assessments. This role will deliver ideation and prototyping, establishing requirements/specifications and verification of performance inputs and outputs. </span></span></span></span><ul><li style=\"margin-right:49px;margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Serve as technical team member or lead in project transfers from early-stage teams into formal design control programs, executing projects based on value improvement, line extensions, and compliance on commercialized products.</span></span></span></span></li><li style=\"margin-right:49px;margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Respond to technical field inquiries and perform root-cause investigations on product failures.</span></span></span></span></li><li style=\"margin-right:49px;margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Create, modify, and qualify test methods per FDA and regulatory requirements.</span></span></span></span></li><li style=\"margin-right:49px;margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Establish and/or tune detailed requirements including product specifications and appropriate test methods through activities such as competitive testing, literature review and KOL engagement.</span></span></span></span></li><li style=\"margin-right:49px;margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Author robust component/assembly drawings, specification documents, test protocols and reports.</span></span></span></span></li><li style=\"margin-right:49px;margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Ensure technical activities are properly documented; participate in and contribute to technical discussion sessions to generate new intellectual property.</span></span></span></span><br> </li></ul><br><span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-family:Roboto;\"><span style=\"color:#ed7d31;\">What You’ll Bring</span></span></b></span></span></span><ul><li style=\"margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Bachelor’s degree in engineering, or related discipline and a minimum of 5 years of related experience in the medical device or related regulated industry; or equivalent combination of education and work experience. </span></span></span></span></li><li style=\"margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Experience in endovascular or neurovascular techniques and devices preferred. </span></span></span></span></li><li style=\"margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Statistical Analysis Software (Minitab or similar) and CAD (Solidworks, ProE, similar). </span></span></span></span></li><li style=\"margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Skilled knowledge of machine shop equipment (mill, lathe, drill press, etc.) operation including operation of 3D printing equipment is preferred. </span></span></span></span></li><li style=\"margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Developing knowledge of product design from concept to regulatory marketing approval. </span></span></span></span></li><li style=\"margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Ability to complete projects individually as well as part of a team, exercising judgment within defined procedures and practices to determine appropriate action. </span></span></span></span></li><li style=\"margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Ability to apply learned techniques to analysis/investigation to solve challenges using problem-solving tools and methodologies. </span></span></span></span></li><li style=\"margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Previous experience working with regulated quality systems such as GMPs, ISO 9001, and the MDD. </span></span></span></span></li><li style=\"margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Familiar with Design Control procedures and requirements. </span></span></span></span></li></ul><br><span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-family:Roboto;\"><span style=\"color:#ed8b00;\">Employee Benefits</span></span></b> <span style=\"font-family:Roboto;\">include </span><span style=\"font-family:Roboto;\">a stake in our collective success with stock options, bonus, competitive salaries, a 401k plan, health benefits, generous PTO, and a parental leave program.</span></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-family:Roboto;\">Join Us! </span></b><a href=\"https://imperativecare.com/careers/\" style=\"color:#0000FF;text-decoration:underline;\"><b><span style=\"font-family:Roboto;\"><span style=\"color:#ed8b00;\">Apply Today</span></span></b></a><span class=\"MsoHyperlink\" style=\"color:#0000FF;\"><span style=\"text-decoration:underline;\"><b><span style=\"font-family:Roboto;\"><span style=\"color:#ed8b00;\">.</span></span></b></span></span></span></span></span><br><br><span style=\"font-size:11pt;\"><span style=\"line-height:107%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"font-family:Roboto;\">Salary Range: $132,000 - 150,000/annually</span></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:Roboto;\"><span style=\"color:#202124;\">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. </span></span></span></span></span></span><br> <p>The use of external recruiters/staffing agencies requires prior approval from our Human Resources Department. The Human Resources Department at Imperative Care requests that external recruiters/staffing agencies not to contact Imperative Care employees directly in an attempt to present candidates. Complying with this request will be a factor in determining future professional relationships with Imperative Care.</p>\n\n<p>Imperative Care will not accept unsolicited resumes from any source other than candidates themselves for either current or future positions. Submission of unsolicited resumes in advance of an agreement between the Human Resources Department and the external recruiter/staffing agency does not create any implied obligation on the part of Imperative Care.</p>",
"description_text": "Job Title: Sr R&D Engineer\n Location : This position is based in our Campbell, California offices. This position is full time.\n Why Imperative Care?\n Do you want to make a real impact on patients? Imperative Care is changing the way stroke is treated. As part of our team, you’d be developing breakthroughs that will revolutionize the future of stroke care. Every day, the technologies that we develop at Imperative Care directly impact human lives. Our focus is on the needs of the patient, and they come first in everything we do.\n What You’ll Do\n As a senior professional, this position will use solid knowledge and experience to design, develop and launch innovative endovascular/neurovascular products through conceptualization, design development, verification/validation, and manufacturability assessments. This role will deliver ideation and prototyping, establishing requirements/specifications and verification of performance inputs and outputs. Serve as technical team member or lead in project transfers from early-stage teams into formal design control programs, executing projects based on value improvement, line extensions, and compliance on commercialized products.\n Respond to technical field inquiries and perform root-cause investigations on product failures.\n Create, modify, and qualify test methods per FDA and regulatory requirements.\n Establish and/or tune detailed requirements including product specifications and appropriate test methods through activities such as competitive testing, literature review and KOL engagement.\n Author robust component/assembly drawings, specification documents, test protocols and reports.\n Ensure technical activities are properly documented; participate in and contribute to technical discussion sessions to generate new intellectual property.\n What You’ll Bring Bachelor’s degree in engineering, or related discipline and a minimum of 5 years of related experience in the medical device or related regulated industry; or equivalent combination of education and work experience.\n Experience in endovascular or neurovascular techniques and devices preferred.\n Statistical Analysis Software (Minitab or similar) and CAD (Solidworks, ProE, similar).\n Skilled knowledge of machine shop equipment (mill, lathe, drill press, etc.) operation including operation of 3D printing equipment is preferred.\n Developing knowledge of product design from concept to regulatory marketing approval.\n Ability to complete projects individually as well as part of a team, exercising judgment within defined procedures and practices to determine appropriate action.\n Ability to apply learned techniques to analysis/investigation to solve challenges using problem-solving tools and methodologies.\n Previous experience working with regulated quality systems such as GMPs, ISO 9001, and the MDD.\n Familiar with Design Control procedures and requirements.\n Employee Benefits include a stake in our collective success with stock options, bonus, competitive salaries, a 401k plan, health benefits, generous PTO, and a parental leave program.\n Join Us! Apply Today .\n Salary Range: $132,000 - 150,000/annually\n 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.\n The use of external recruiters/staffing agencies requires prior approval from our Human Resources Department. The Human Resources Department at Imperative Care requests that external recruiters/staffing agencies not to contact Imperative Care employees directly in an attempt to present candidates. Complying with this request will be a factor in determining future professional relationships with Imperative Care.\n Imperative Care will not accept unsolicited resumes from any source other than candidates themselves for either current or future positions. Submission of unsolicited resumes in advance of an agreement between the Human Resources Department and the external recruiter/staffing agency does not create any implied obligation on the part of Imperative Care.",
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"description": "<span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-size:12pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Job Title: Sr R&D Engineer </span></span></span></b></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-family:Roboto;\">Location</span></b><i><span style=\"font-family:Roboto;\">: This position is based in our Campbell, California offices. This position is <u>full time.</u></span></i></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-family:Roboto;\"><span style=\"color:#ed7d31;\">Why Imperative Care?</span></span></b></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"font-family:Roboto;\">Do you want to make a real impact on patients? Imperative Care is changing the way stroke is treated. As part of our team, you’d be developing breakthroughs that will revolutionize the future of stroke care. Every day, the technologies that we develop at Imperative Care directly impact human lives. Our focus is on the needs of the patient, and they come first in everything we do.</span></span></span></span><br><br><span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-family:Roboto;\"><span style=\"color:#ed7d31;\">What You’ll Do</span></span></b></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"font-family:Roboto;\">As a senior professional, this position will use solid knowledge and experience to design, develop and launch innovative endovascular/neurovascular products through conceptualization, design development, verification/validation, and manufacturability assessments. This role will deliver ideation and prototyping, establishing requirements/specifications and verification of performance inputs and outputs. </span></span></span></span><ul><li style=\"margin-right:49px;margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Serve as technical team member or lead in project transfers from early-stage teams into formal design control programs, executing projects based on value improvement, line extensions, and compliance on commercialized products.</span></span></span></span></li><li style=\"margin-right:49px;margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Respond to technical field inquiries and perform root-cause investigations on product failures.</span></span></span></span></li><li style=\"margin-right:49px;margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Create, modify, and qualify test methods per FDA and regulatory requirements.</span></span></span></span></li><li style=\"margin-right:49px;margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Establish and/or tune detailed requirements including product specifications and appropriate test methods through activities such as competitive testing, literature review and KOL engagement.</span></span></span></span></li><li style=\"margin-right:49px;margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Author robust component/assembly drawings, specification documents, test protocols and reports.</span></span></span></span></li><li style=\"margin-right:49px;margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Ensure technical activities are properly documented; participate in and contribute to technical discussion sessions to generate new intellectual property.</span></span></span></span><br> </li></ul><br><span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-family:Roboto;\"><span style=\"color:#ed7d31;\">What You’ll Bring</span></span></b></span></span></span><ul><li style=\"margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Bachelor’s degree in engineering, or related discipline and a minimum of 5 years of related experience in the medical device or related regulated industry; or equivalent combination of education and work experience. </span></span></span></span></li><li style=\"margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Experience in endovascular or neurovascular techniques and devices preferred. </span></span></span></span></li><li style=\"margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Statistical Analysis Software (Minitab or similar) and CAD (Solidworks, ProE, similar). </span></span></span></span></li><li style=\"margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Skilled knowledge of machine shop equipment (mill, lathe, drill press, etc.) operation including operation of 3D printing equipment is preferred. </span></span></span></span></li><li style=\"margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Developing knowledge of product design from concept to regulatory marketing approval. </span></span></span></span></li><li style=\"margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Ability to complete projects individually as well as part of a team, exercising judgment within defined procedures and practices to determine appropriate action. </span></span></span></span></li><li style=\"margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Ability to apply learned techniques to analysis/investigation to solve challenges using problem-solving tools and methodologies. </span></span></span></span></li><li style=\"margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Previous experience working with regulated quality systems such as GMPs, ISO 9001, and the MDD. </span></span></span></span></li><li style=\"margin-left:8px;\"><span style=\"font-size:12pt;\"><span style=\"font-family:'New York', serif;\"><span style=\"font-size:11pt;\"><span style=\"font-family:Roboto;\">Familiar with Design Control procedures and requirements. </span></span></span></span></li></ul><br><span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-family:Roboto;\"><span style=\"color:#ed8b00;\">Employee Benefits</span></span></b> <span style=\"font-family:Roboto;\">include </span><span style=\"font-family:Roboto;\">a stake in our collective success with stock options, bonus, competitive salaries, a 401k plan, health benefits, generous PTO, and a parental leave program.</span></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-family:Roboto;\">Join Us! </span></b><a href=\"https://imperativecare.com/careers/\" style=\"color:#0000FF;text-decoration:underline;\"><b><span style=\"font-family:Roboto;\"><span style=\"color:#ed8b00;\">Apply Today</span></span></b></a><span class=\"MsoHyperlink\" style=\"color:#0000FF;\"><span style=\"text-decoration:underline;\"><b><span style=\"font-family:Roboto;\"><span style=\"color:#ed8b00;\">.</span></span></b></span></span></span></span></span><br><br><span style=\"font-size:11pt;\"><span style=\"line-height:107%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"font-family:Roboto;\">Salary Range: $132,000 - 150,000/annually</span></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:Roboto;\"><span style=\"color:#202124;\">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. </span></span></span></span></span></span><br> <p>The use of external recruiters/staffing agencies requires prior approval from our Human Resources Department. The Human Resources Department at Imperative Care requests that external recruiters/staffing agencies not to contact Imperative Care employees directly in an attempt to present candidates. Complying with this request will be a factor in determining future professional relationships with Imperative Care.</p>\n\n<p>Imperative Care will not accept unsolicited resumes from any source other than candidates themselves for either current or future positions. Submission of unsolicited resumes in advance of an agreement between the Human Resources Department and the external recruiter/staffing agency does not create any implied obligation on the part of Imperative Care.</p>",
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