Careers

Please navigate to desired department to view open positions and fill out form below to request to apply.

Accounting & Finance

Senior Manager, Corporate Tax

As a dedicated tax professional working independently, the Senior Manager, Corporate Tax will be the subject matter expert to the department and help build the tax function within the organization, while applying knowledge to a wide range of tax areas and processes. 

To learn more and apply, please click here.

    Clinical

    Associate Director, Clinical Insights

    Job Summary

    The Associate Director of Clinical Insights will lead the strategy and execution surrounding data analytics of internal and external data sources to provide actionable clinical insights for key stakeholders. This role will be the functional domain expert and drive data analytic efforts to provide product and procedural insights to internal teams and ultimately help optimize definitive study designs in the field.

    Qualifications

    •  Master’s degree, Ph.D. in biological/clinical science or engineering, or M.D. with a minimum of five years of medical device/medical products industry experience
    • Proficient written and oral communication and presentation skills
    • Strong analytic abilities to understand, digest, and summarize complex data to different audiences
    • Ideally has prior experience working with healthcare economics databases
    • Must have a good understanding of the medical environment to effectively respond to market concerns and provide technical support for products
    • Ability to become a domain expert in complex and evolving disease landscapes (e.g., pulmonary embolism and deep vein thrombosis)
    • Ability to plan and manage at both strategic and tactical levels
    • Strong project management and organizational skills
    • Ability to work on multiple projects simultaneously and be flexible enough to change priorities with short notice when necessary
    • Ability to competently represent Inari at professional functions and customer meetings
    • Must be able to work independently with minimal direction
    • A healthy disdain for the status quo, and a willingness to question existing practices to identify better alternatives
    • Ability to succeed in a rapidly changing, agile environment where continuous innovation is requisite to success
    • Excellent advocacy and persuasive skills
    • Ability to succeed and be effective in a fast-paced, entrepreneurial environment
    • Proficient software skills across all standard programs

    Senior Clinical Research Associate

    Job Summary: 

    Responsible for all clinical site management activities in the U.S. following good clinical practice and all applicable regulations.  This position will work collaboratively with the external Contract Research Organization, additional study team members, customers, and other internal partners enabling patient access to advanced care of their venous thromboembolism. 

    Qualifications: 

    • Perform all aspects of site nomination, selection, confirmation, execution, data collection, monitoring, and closure activities.
    • Develop strong customer relationships ensuring appropriate sponsor oversight of clinical research centers.
    • Drive site recruitment strategies, data quality, and patient compliance to protocol.
    • Partner with study team to develop all study documents necessary for trial execution.
    • Contribute to drafting of protocols, patient informed consent forms and case report forms.
    • Deliver site training, updates, and study communication materials to sites.
    • Manage site payments, study contracts, consent approvals, IRB approvals, and other research processes with sites.
    • Maintain compliance to all SOP, GCP, and regulatory processes.
    • Ensure highest level of data quality at the site including driving resolution of queries.
    • Strong technical knowledge of Inari products and procedures.
    • Strong clinical process acumen and ability to drive clinical excellence activities.
    • Monitor selected sites through source data verification, Conduct Site Initiation Visits, Interim Monitoring visits, and close out visits.
    • Drive high quality data collection to support scientific communications, clinical research, and statistics evidence dissemination strategies.

      Manager, Statistical Programming  

      Job Summary:  

      This position will be primarily responsible for statistical programming, analysis of clinical research studies, and providing programming support of publication efforts and regulatory submissions. 

      Qualifications:  

      • MS in Statistics, Mathematics, or related fields.
      • 4+ years relevant work experience with statistical analysis and interpretation of data.
      • 3+ years relevant industry experience in Pharma, Med Device, CRO.
      • 3+ years clinical trial experience.
      • 3+ years clinical database experience and CDISC pipeline process.
      • Comprehensive knowledge of statistical methods.
      • Comprehensive knowledge of mathematical modeling.
      • Knowledge of software development packages (SAS, R, or other software packages).
      • Strong project management and problem-solving skills, and ability to effectively lead and collaborate with all functions.
      • High attention to detail including proven ability to manage multiple, competing priorities.
      • Proficiency in MS Office Suite including Word, PowerPoint, Access, and Excel.
      • Ability to manage multiple projects simultaneously.

      Statistical Programmer II

      Job Summary:

      This position will be primarily responsible for statistical programming, analysis of clinical research studies, and providing programming support of publication efforts and regulatory submissions.

      Qualifications: 

      • MS in Statistics, Mathematics, or related fields.
      • 2+ years relevant work experience in statistical analysis and interpretation of data.
      • 2+ years relevant industry experience in Pharma, Med Device, CRO.
      • 2+ years clinical trial experience.
      • 2+ years clinical database experience and CDISC pipeline process.
      • Working knowledge of statistical methods.
      • Working knowledge of mathematical modeling.
      • Knowledge of software development packages (SAS, R, or other software packages).
      • Strong project management and problem-solving skills, and ability to effectively lead and collaborate with all functions.
      • High attention to detail including proven ability to manage multiple, competing priorities.
      • Proficiency in MS Office Suite including Word, PowerPoint, Access, and Excel.
      • Ability to manage multiple projects simultaneously.

      Principal Biostatistician   

      Job Summary: 

      This position will be primarily responsible for statistical design, analysis of clinical research studies, and providing statistical expertise in support of publication efforts and regulatory submissions.

      Qualifications: 

      • Ph.D. in Statistics, Biostatistics, or related fields.
      • Minimum 4-6 years of experience in clinical trials.
      • Computer science/programming education and experience strongly desired.
      • Proficiency in SAS and/or R statistical software.
      • Proficiency in data programming to facilitate statistical analyses.
      • Proficiency in MS Office Suite including Word, PowerPoint, Access, and Excel
      • Ability to manage multiple projects simultaneously.
      • Managerial track preferred.

      Commercial

      Associate Marketing Manager:

      Job Summary:

      The primary focus for the Marketing Associate is to provide comprehensive marketing support to ensure assigned product’s success in the marketplace. This support includes projects to optimize sales communication, product development, physician/new hire training, and product positioning/promotion.  In addition, the Marketing Associate will support marketing events and programs ensuring VOC is heard. This position must be able to communicate with all areas of the company and will interact on a regular basis with QA/RA, Clinical, Marketing, Sales, Engineering, Customers, and Senior Leadership.

      Qualifications:

      • Bachelor’s Degree preferably in marketing, business, biological/clinical science, or engineering, MBA a plus, with a minimum of one (1) year of medical device/medical products marketing experience. Medical device sales experience is a plus.
      • Excellent communication and presentation skills
      • Must have a good understanding of the medical environment to effectively respond to market concerns and provide technical support for products
      • Able to convert product/customer feedback into valuable insights that can help drive the development of new marketing programs
      • Ability to competently represent the Company at professional functions and customer meetings
      • Excellent advocacy and persuasive skills
      • Proficient software skills across all standard programs; Salesforce.com experience a plus
      • Must be able to work independently with minimal direction
      • A healthy disdain for the status quo, and a willingness to question existing practices to identify better alternatives
      • Ability to work on multiple projects simultaneously and be flexible enough to change priorities with short notice when necessary
      • Ability to succeed in a rapidly changing, agile environment where continuous innovation is requisite to success
      • Ability to plan and manage at both strategic and tactical levels
      • Strong project management and organizational skills
      • Ability to succeed and be effective in a fast-paced, entrepreneurial environment

      For inquiries on this role please email product-marketing@inarimedical.com with resume attached.  Currently, there are openings for an Upstream (Product Development) role or a Downstream (Market Development) role; please specify which is preferable.

      Data Intelligence Analyst

      Job Summary:

      The Data Intelligence Analyst works independently with designing and maintaining data systems, including driving data warehousing efforts and responsible for developing and maintaining extract, transform, and load data feeds/transfers through Business Intelligence reports and dashboards.

      Qualifications:

      • Bachelor’s degree in Information Systems, Management Information Systems, or related field. A minimum of 5+ years in related role in medical device, pharmaceuticals, or any life science industry
      • Minimum of five-year experience with SQL Server Management Studio
      • Strong experience in SQL Server Reporting Services
      • Strong experience in Tableau
      • Strong experience with development of ETL processes
      • Ability to thrive in a demanding, change-oriented, fast paced environment requiring a high degree of deadline-driven productivity
      • Ability to meet deadlines and handle and prioritize multiple requests
      • Able to identify upstream and downstream impact analysis through applications, systems, and processes.
      • Ability to work independently and manage multiple projects while meeting deadlines

      Marketing Coordinator

      Job Summary:

      The Marketing Coordinator, under direct supervision, is responsible for assisting the rapidly expanding commercial team by supporting the planning and coordination of events/conferences/tradeshows, managing inventory, and other marketing administrative support.

      Qualifications:

      • Bachelor’s degree in Marketing, Communications, or related field.
      • Minimum 2+ years’ experience in a fast-paced environment.
      • Proficiency with Microsoft PowerPoint, Word, and Excel.
      • Experience with Adobe InDesign and Adobe Premiere Pro; preferred.
      • Strong written and verbal communication skills.
      • Ability to be self-motivated and work as part of a team.
      • Strong attention to detail, excellent time management, and organization/planning skills.

      Customer Service

      There are no open positions at this time.

        Engineering

        Senior R&D Technician

        Job Summary

        Supports product development by testing, troubleshooting, and documenting new product components, processes, and equipment, as directed.

        Responsibilities

        • Fabricate prototypes, manufacturing processes, and fixtures from verbal instructions and/or simple drawings
        • Set up and conduct tests of completed units or components under operational conditions to investigate designs or to obtain data for development and standardization
        • Assist with the development and improvement of new and existing test protocols
        • Record and analyze test procedures and results, numerical and graphical data
        • Support production or process development as required
        • Assemble, install, adjust, test, and operate laboratory equipment and instruments

        Qualifications

        •  Computer skills including Excel, Word, and preferably some AutoCAD and SolidWorks
        • Knowledge of materials and suppliers
        • Good written and oral communication
        • Knowledge of good laboratory and documentation practices
        • High School Diploma or equivalent; some college coursework preferred
        • Five or more years’ experience as a technician in medical device industry

        Senior R&D Project Engineer

        Job Summary

        Support and lead teams in the development of medical device products, including writing or verifying specifications, maintaining product process, designing fixtures, test processes, equipment and raw materials to ensure the concepts and/or prototypes meet their requirements.

        Responsibilities

        • Develop new product concepts and products
        • Engineering design and process development
        • Generate intellectual property, write invention disclosures
        • Specifies and/or directs the specification and testing of new materials and designs.
        • Confers with appropriate departments, resources, and/or outside services to prepare design modifications, clarify problems and develop designs
        • Largely self-directed, capable of meeting project goals with minimal supervision

        Qualifications

        • BS degree in related field
        • 5-10 years related medical device experience
        • Good communication skills
        • Design and development of medical devices
        • Reading and preparing technical documentation
        • Working knowledge of standard machine shop equipment and processes and medical device manufacturing equipment and processes
        • Knowledge of medical and technical development
        • Computer skills including Word, Excel and AutoCAD (Solidworks proficiency required)

        Human Resources

        Benefits Specialist

        The Benefits Specialist is responsible for assisting with the administration of all benefits and retirement programs, including medical, dental, vision, life insurance, short- and long-term disability, leaves of absence, and 401(k) plan on a professional level. Works closely with the Benefits Manager in supporting all team members. 

        To learn more and apply, please click here.

         

        IT

        IT Systems & Data Analyst

        The IT Systems & Data Analyst is responsible for designing, implementing and managing new technology solutions to improve business efficiency and productivity. The work will primarily be for an internal client within the company. The IT Systems & Data Analyst works closely with the client to examine existing business models and flows of data, discuss their findings with the client, and design an appropriate improved IT solution. They act as the liaison between the internal and external teams. Demonstrates expertise in a variety of the field’s concepts, practices, and procedures. Relies on extensive experience and judgment to plan and accomplish goals. Performs a variety of tasks and can function as a implementation project manager when needed. A wide degree of creativity and latitude is expected. This is an individual contributor position that offers specialized expertise to internal and external project teams, without the need to be managing a team of people.

        To learn more and apply, please click here.

        Software Quality Engineer

        The Software Quality Engineer will play a key role in the various business system software implementation and maintenance by driving quality improvements and validating quality criteria.  This role will also have a broad range of responsibilities in project management and compliance.

        To learn more and apply, please click here.

        Legal

        There are no open positions at this time.

        Production

        Assembler

        Essential Responsibilities:

        • Using a variety of tools, fixtures, work instructions and test equipment perform a series of operations to correctly assemble/test medical devices.
        • Understand and follow detailed assembly instructions, processes and procedures.
        • Comply with policies, guidelines and regulatory requirements per the Quality System.
        • Provide hands on job function training to coworkers as needed.
        • Maintain a clean and organized work area to facilitate manufacturing functions.

        Qualifications:

        • High school diploma or equivalent.
        • 1 to 5 years related medical device manufacturing experience.
        • Able to work in a cleanroom environment.
        • Knowledge of basic measuring techniques including scales, rulers, US and metric measurements.

         

        Warehouse Associate I

        Coordinates the day-to-day inventory control responsibilities, the incoming and outgoing process of products, and the accuracy of inventory records and transactions.

        Essential Responsibilities:

        • Performs routine cycle counts.
        • Data entry of inventory transactions and cycle count results into ERP system.
        • Pulls inventory items based on pick lists for production work orders.
        • Assist in the Investigates quantity discrepancies with manufacturing, production, and inspection personnel.
        • Prepares and participates in year-end physical inventory.
        • Asist in monitor and maintain appropriate inventory levels of all cleanroom supplies and warehouse supplies.
        • Receives, unpacks, and delivers goods; re-stocks items as necessary in cleanroom, warehouse, shipping dept.
        • Processes and documents FG’s returns per company’s established procedures.
        • Performs routine clerical duties, including data entry.  Performs miscellaneous job-related duties and special projects as assigned.

        Qualifications:

        • High School Diploma.
        • Minimum of 1 year Inventory Control experience.
        • Must be computer literate.
        • Must be detail-oriented and pay close attention to accuracy.
        • Able to properly handle confidential information and records.
        • Able to analyze information gathered in order to identify potential problems or discrepancies.
        • Knowledge of supplies, equipment, and/or services ordering and inventory control.

        Quality & Regulatory

        There are no open positions at this time.

        Careers Contact

        Please leave a message or reach out to email below with resume attached.
        HR@inarimedical.com
        9 Parker, Suite 100

        Irvine, CA 92618

        Request to Apply

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