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    <title>InspireMD Jobs</title>
    <link>https://portal.brightmove.com/CompanyPortal.do?companyGK=53774&amp;portalGK=44115</link>
    <description><![CDATA[Job Postings available for application.]]></description>
    <language>en-us</language>
    <pubDate>Sat, 07 Mar 2026 09:56:58 EST</pubDate>
    <lastBuildDate>Sat, 07 Mar 2026 09:56:58 EST</lastBuildDate>
    <generator>BrightMove ATS</generator>
    <item>
      <title><![CDATA[Office Administrator - Miami, FL]]></title>
      <link>https://portal.brightmove.com/jb.do?reqGK=27772286&amp;companyGK=53774&amp;portalGK=44115</link>
      <guid>a356fd1f-1e7f-46da-8366-0eb1d5531cc4</guid>
      <description><![CDATA[Work Arrangement: On-Site
Hours: Monday to Friday, 8:00 AM to 5:00 PM



Position Summary
The Office Administrator is responsible for supporting the day-to-day office operations for a growing Medical Device company by performing a variety of clerical and administrative tasks. You'll be highly adaptable and eager to jump in wherever needed, supporting daily operations and cross-team initiatives to keep the business moving during periods of rapid change.


Essential Duties and Responsibilities

Highly adaptable and eager to jump in wherever needed, supporting daily operations and cross-team initiatives to keep the business moving during periods of rapid change.
Provide a welcoming environment to clients by preparing the conference room prior to meetings, welcoming visitors, and notifying appropriate team members of arrival.
Manage the kitchen break room: Order and stock groceries, manage coffee maker, clean/put away dishes, and manage organization.
Accept and distribute mail/packages.
Maintain office supply inventory, completing order requests as needed.
Support staff projects as needed, preparing PowerPoint decks, organizing data into Excel spreadsheets, and obtaining meeting minutes as needed.



Required Qualifications

At least 2 years of experience, preferably in an administrative or similar environment wearing multiple hats.
High School Diploma. Associates degree is preferred.
Experience with establishing vendor purchase orders and invoicing.
Proficient in Microsoft Office Suite (Excel, Word, PowerPoint) with strong technical skills.
Strong communication skills, both written and verbal.
Detail-oriented with the ability to manage multiple tasks and meet deadlines.
Ability to work independently and collaboratively in a small team environment.
Bilingual: English & Spanish is preferred.



About This Opportunity
This is a fantastic opportunity to join a growing Medical Device company where your contributions will be directly valued. You'll work in a collaborative, fast-paced environment where your organizational skills and can-do attitude will help shape our company culture. If you're someone who thrives on variety, enjoys supporting a team, and takes pride in keeping operations running smoothly, this role is perfect for you.]]></description>
      <pubDate>Thu, 26 Feb 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Office Administrator - Part-Time - Miami, FL]]></title>
      <link>https://portal.brightmove.com/jb.do?reqGK=27772304&amp;companyGK=53774&amp;portalGK=44115</link>
      <guid>fe996c5d-cb0e-4ef4-b291-81504a83bcc0</guid>
      <description><![CDATA[Work Arrangement: Part-Time, On-Site



Position Summary
Join our growing Medical Device company as an Office Administrator and become an essential part of our dynamic team. In this role, you'll support our day-to-day office operations by performing a variety of clerical and administrative tasks. You'll be the backbone of our office, ensuring smooth operations and creating a welcoming environment for both team members and clients. If you're highly adaptable, detail-oriented, and eager to make an impact, we'd love to meet you.


Essential Duties and Responsibilities

Be highly adaptable and eager to jump in wherever needed, supporting daily operations and cross-team initiatives to keep the business moving during periods of rapid change
Provide a welcoming environment to clients by preparing the conference room prior to meetings, greeting visitors, and notifying appropriate team members of their arrival
Manage the kitchen break room by ordering and stocking groceries, maintaining the coffee maker, cleaning and organizing dishes, and ensuring the space remains organized and inviting
Accept and distribute mail and packages promptly and accurately
Maintain office supply inventory and complete order requests as needed to keep operations running smoothly
Support staff projects as needed, including preparing PowerPoint presentations, organizing data into Excel spreadsheets, and obtaining meeting minutes



Required Qualifications

At least 2 years of experience in an administrative or similar environment, with experience wearing multiple hats
High School Diploma (Associates degree preferred)
Experience establishing vendor purchase orders and managing invoicing
Proficient in Microsoft Office Suite (Excel, Word, PowerPoint) with strong technical skills
Strong communication skills, both written and verbal
Detail-oriented with the ability to manage multiple tasks and meet deadlines
Ability to work independently and collaboratively in a small team environment



About This Opportunity
This is a fantastic opportunity to join a growing Medical Device company where your contributions will be directly valued. You'll work in a collaborative, fast-paced environment where your organizational skills and can-do attitude will help shape our company culture. If you're someone who thrives on variety, enjoys supporting a team, and takes pride in keeping operations running smoothly, this role is perfect for you.]]></description>
      <pubDate>Thu, 26 Feb 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Senior Process Engineer - Charlotte, NC]]></title>
      <link>https://portal.brightmove.com/jb.do?reqGK=27771509&amp;companyGK=53774&amp;portalGK=44115</link>
      <guid>130e0c4d-fd3b-43d9-b535-96170fae9bdc</guid>
      <description><![CDATA[Senior Process Engineer

Location: Charlotte, North Carolina
Work Arrangement: Hybrid (with regular visits to contract manufacturer and travel to Miami headquarters as required)



Job Summary
InspireMD is establishing a second manufacturing line in the United States for the CGuard Prime product, which has recently launched in the United States. The person in this role will lead all manufacturing process improvement and capacity expansion initiatives at InspireMD's contract manufacturer in Charlotte, North Carolina. Additionally, this individual will become the US-Based Subject Matter Expert for all processes related to the manufacturing and assembly of InspireMD products.
InspireMD headquarters is located in Miami, Florida, and the manufacturing location is Charlotte, NC. This position offers a hybrid work arrangement with regular visits to our contract manufacturer as required, as well as travel to Miami to interface with the Miami-based leadership team.


Essential Duties and Responsibilities
Process Knowledge and Equipment Transfer



Quickly understand all equipment and processes related to the manufacturing of InspireMD products including catheter processing and assembly, mesh knitting, stent crimping, final assembly, and more
Maintain working knowledge of medical device component processing including nitinol laser cutting, injection molding, catheter processing, and related technologies
Identify and address inefficiencies in current processes to improve productivity and reduce costs
Work collaboratively with our contract manufacturing partner to lead process and continuous improvement initiatives
Utilize Six Sigma, Lean, and other process improvement methodologies to enhance process performance



Compliance & Quality Assurance



Ensure all activities comply with InspireMD quality requirements
Collaborate with Quality Assurance to address any deviations and implement corrective actions



Cross-Functional Collaboration



Work closely with R&D, Production, and Supply Chain teams to support the transition of new products from development to manufacturing
Provide technical support and training to the CMO to ensure smooth operation and adherence to process standards



Data Analysis & Reporting



Prepare and present reports on product transfer, process improvement initiatives, and project status to management



Project Management



Serve as the primary liaison between the CMO and the Tel Aviv team to ensure all manufacturing process-related activities are properly executed
Lead and participate in product transfer and process improvement projects, ensuring timely and successful completion
Manage project timelines and budgets to meet project objectives





Required Qualifications



Bachelor's degree in mechanical engineering with strong mechanical acumen
Proven experience as a Product or Process Development Engineer in the medical devices industry with a minimum of 8 years' experience
Strong knowledge of manufacturing processes, equipment, and technologies specific to medical devices
Experience working closely with product development teams to provide Design for Manufacturing (DFM) guidance
Familiarity with FDA regulations, ISO 13485, and other industry standards
Proficiency in process improvement methodologies such as Six Sigma and Lean
Excellent analytical, problem-solving, and project management skills
Strong communication and interpersonal skills with the ability to work effectively in a team environment
Ability to travel domestically and internationally (Europe and Israel) to understand current component and assembly equipment and processes, approximately 25-50% travel as needed





About This Opportunity
This is a pivotal role for a growing medical device company expanding its US manufacturing capabilities. You will have the opportunity to shape manufacturing processes from the ground up, work with cutting-edge medical device technologies, and make a direct impact on product quality and company growth. If you're an experienced process engineer looking to take on a leadership role and drive meaningful improvements in a dynamic environment, we want to hear from you.]]></description>
      <pubDate>Mon, 16 Feb 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Field Clinical Specialist - Morristown, NJ]]></title>
      <link>https://portal.brightmove.com/jb.do?reqGK=27767550&amp;companyGK=53774&amp;portalGK=44115</link>
      <guid>4525E37C-6D5B-3EB4-E063-0100007F8544</guid>
      <description><![CDATA[Field Clinical Specialist - (Morristown)
Remote/Field roleInspireMD is a dynamic growing company focused on developing and commercializing innovative Class III PMA and Class II medical devices. We are seeking a Field Clinical Specialist (FCS) to join our team. In this role, you will be responsible for providing world class training, case planning and support to customers using or interested in using InspireMD products.  Reporting to a Regional Sales Director, the FCS will work with Territory Managers (TMs), fellow FCSs and other functions (Training/Commercial Development, Clinical Affairs, etc.) to support customers in both the clinical and commercial settings to support the overall success of InspireMD&rsquo;s launches of CGuard Prime and SwitchGuard.Key Responsibilities:A Field Clinical Specialist is responsible for providing world class training, case planning and support to customers using or interested in using InspireMD products.Support and influence all customer types- (Interventional, Vascular, and Neuro Interventional, supporting both CAS and TCAR procedures to optimize patient outcomes, to include the creation of case plans.Collaborate with RSD and TMs to target and maximize CAS, TCAR and neuro (to include tandem lesion) opportunities, as product approvals and launches allow.Collaborate with commercial development to enhance professional education (physician/customer) programs as requested.Collaborate with Clinical Affairs to provide outstanding case support for clinical trials, as requested.Leverage and build customer relationships to support commercialization/product launch, professional education, and field training efforts.Inspection Support: Support FDA inspections and audits, ensuring that all regulatory and complaint handling documentation is in order and facilitating smooth interactions with regulatory authorities.Qualifications:Minimum of five (5) years of experience in the medical device industry or clinical/patient care, including prior experience with Interventional Cardiology/Radiology/Neurology and/or Vascular Surgery.Prior experience with innovative medical products; Endovascular experience.Educational degree or certification in a business, life sciences or a healthcare discipline.]]></description>
      <pubDate>Thu, 04 Dec 2025 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Field Clinical Specialist - Atlanta, GA]]></title>
      <link>https://portal.brightmove.com/jb.do?reqGK=27766972&amp;companyGK=53774&amp;portalGK=44115</link>
      <guid>440DDA61-5976-7DBF-E063-0100007FD869</guid>
      <description><![CDATA[Field Clinical Specialist 
Remote/Field role
InspireMD is a dynamic growing company focused on developing and commercializing innovative Class III PMA and Class II medical devices. We are seeking a Field Clinical Specialist (FCS) to join our team. In this role, you will be responsible for providing world class training, case planning and support to customers using or interested in using InspireMD products.  Reporting to a Regional Sales Director, the FCS will work with Territory Managers (TMs), fellow FCSs and other functions (Training/Commercial Development, Clinical Affairs, etc.) to support customers in both the clinical and commercial settings to support the overall success of InspireMD&rsquo;s launches of CGuard Prime and SwitchGuard.
Key Responsibilities:

A Field Clinical Specialist is responsible for providing world class training, case planning and support to customers using or interested in using InspireMD products.
Support and influence all customer types- (Interventional, Vascular, and Neuro Interventional, supporting both CAS and TCAR procedures to optimize patient outcomes, to include the creation of case plans.
Collaborate with RSD and TMs to target and maximize CAS, TCAR and neuro (to include tandem lesion) opportunities, as product approvals and launches allow.
Collaborate with commercial development to enhance professional education (physician/customer) programs as requested.
Collaborate with Clinical Affairs to provide outstanding case support for clinical trials, as requested.
Leverage and build customer relationships to support commercialization/product launch, professional education, and field training efforts.
Inspection Support: Support FDA inspections and audits, ensuring that all regulatory and complaint handling documentation is in order and facilitating smooth interactions with regulatory authorities.

Qualifications:

Minimum of five (5) years of experience in the medical device industry or clinical/patient care, including prior experience with Interventional Cardiology/Radiology/Neurology and/or Vascular Surgery.
Prior experience with innovative medical products; Endovascular experience.
Educational degree or certification in a business, life sciences or a healthcare discipline.]]></description>
      <pubDate>Thu, 20 Nov 2025 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Principal Biostatistician - Miami, FL,]]></title>
      <link>https://portal.brightmove.com/jb.do?reqGK=27754065&amp;companyGK=53774&amp;portalGK=44115</link>
      <guid>32EB4A12-FF48-5391-E063-0100007FAB53</guid>
      <description><![CDATA[Position Summary: The Principal Biostatistician will use statistical expertise in study design and analysis of data to support the generation of evidence for regulatory and commercial needs.Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform the following satisfactorily; other duties may be assigned. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.Development of Statistical Analysis Plans including statistical methodology, definition of derived variables, data-handling rules, mockups and ultimately analysis of study data in support of business needs.Participate in the design and execution of global studies for regulatory submissions, reimbursement, and product adoption, including clinical study documents (protocol, case report forms, etc.), study implementation and data managementStatistical programming of deliverables for regulatory submissions, including specification and delivery of integrated databases, outputs, and response to regulatory questions.Lead analysis for publications or podium presentations.Develop SAS macros, templates and utilities for data reporting and visualization.Write and validate SAS programs to generate tables, listings, and figures (TLFs) for clinical study reports and analysis of datasets.Proactively seek out and follow best practices in programming documentation.Lead the statistical programming thinking, analysis, and reporting to relevant groups in product and study teams.Regularly communicates study status to senior management and represents the organization to key customers.Other duties as assigned.Requirements: To perform the job successfully, an individual should demonstrate the following.Master's degree in Biostatistics or Epidemiology and 8+ years of direct and related experience in medical device, pharmaceutical, biotechnology or PhD and 6+ years of experience.Working Knowledge of Good Clinical Practice (GCP) and regulatory compliance guidelines for clinical trials.Proficiency in SAS and SAS macros that includes the fuse of a variety of statistical procedures, e.g., nonparametric analysis, linear and non-linear models, categorical data and survival analysis required.Experience with analysis of medical device trials for PMA or 510(k) preferred.Excellent critical thinking skills.Experience in product safety including serving on DSMBs preferred.Ability to perform and interpret subgroup analyses.Ability to work effectively on cross-functional teams.Experience with Statistical modeling: Kaplan-Meier, Bayesian analysis.Effective communication skills with all levels of management.Can operate within a team and independently, with adaptability to changing requirements.Education/Experience:Master&rsquo;s degree in Biostatistics or Epidemiology and 8+ years of direct and related experience in medical device, pharmaceutical, biotechnology industry or PhD and 6+ years of experience.The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their supervisor.]]></description>
      <pubDate>Wed, 16 Apr 2025 00:00:00 EDT</pubDate>
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