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Sr R&D Engineer

Imperativecare · Campbell, CA, 95008 · Active · $132,000 / year · JazzHR / ApplyToJob

Job facts

FieldValue
CompanyImperativecare
TitleSr R&D Engineer
Normalized title-
Department / team-
LocationCampbell, CA, United States
Work model-
Employment typeFull Time
Salary$132,000 / year
Statusactive
ATS providerJazzHR / ApplyToJob
Posted / first seen2026-04-21 / 2026-05-30
Changed / last seen2026-05-30 / 2026-06-06

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PageWhat it containsOpen
Company jobsActive postings from Imperativecare.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through JazzHR / ApplyToJob.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Campbell.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyImperativecare
Sourcecade5286-aa33-4e90-940f-d7a3fd45cd44
ATS providerJazzHR / 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 IDb3c2eefdf7d4cc8d0ff51591f9fc42cf2cb4a221
Org IDb2419ccb-c14b-43dc-b827-465290ac8fd3
Source IDcade5286-aa33-4e90-940f-d7a3fd45cd44
Board IDcade5286-aa33-4e90-940f-d7a3fd45cd44
Providerjazzhr
Provider Job Keyk4RwubZAks
TitleSr R&D Engineer
Normalized Title
Statusactive
Activeyes
Location TextCampbell, CA, 95008
Department
Team
Employment Typefull_time
Workplace Type
Remote Policy
CountryUnited States
RegionCA
CityCampbell
Salary RawSalary Range: $132,000 - 150,000/annually Please note that the salary information is a general guideli
Salary Min132,000
Salary Max
Salary CurrencyUSD
Salary Periodyear
Source URLhttps://imperativecare.applytojob.com/apply/k4RwubZAks/Sr-RD-Engineer
Apply URLhttps://imperativecare.applytojob.com/apply/k4RwubZAks/Sr-RD-Engineer
First Seen At2026-05-30 06:05:28Z
Last Seen At2026-06-06 10:50:38Z
Last Checked At2026-06-06 10:50:38Z
Last Changed At2026-05-30 06:05:28Z
Inactive At
Source Posted At2026-04-21 00:00:00Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=jazzhr/board=imperativecare/date=2026-06-06/2026-06-06T10-50-36-289Z-9978bb13ad458de8b79e52f4b96ce7232e5c5cb1515c2a8c446a530dda7413c5.json
Event Fields
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  "last_changed_at": "2026-05-30T06:05:28.959Z",
  "active_status": "active"
}
Parsed Structured
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Extensions
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Native Structured
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    "heading": "Sr R&D Engineer",
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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.",
    "jsonld_jobposting": {
      "url": "https://imperativecare.applytojob.com/apply/k4RwubZAks/Sr-RD-Engineer",
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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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