Welcome to the MicroVention Talent Gateway
MicroVention is a rapidly growing medical device company that has pioneered the development of catheter-based, minimally invasive, neuroendovascular technologies that provide therapeutic advantages for neurovascular disorders.
We are a worldwide community of over 2000 engineers, chemists, marketers, manufacturers, researchers, and innovators who share the same ethos — creating technologies that provide a meaningful improvement in patient lives. From the beginning, we sought to develop and market medical devices that would improve the treatment of diseases in small blood vessels. After developing some early concepts and prototypes, our company narrowed its focus to aneurysm therapy, developing a line of implantable, detachable neuroendovascular platinum coils. In 2006, we were acquired by the Japan-based Terumo® Corporation. Terumo provided the framework for MicroVention to operate autonomously and grow freely. Today, we have launched over 30 products and have expanded beyond cerebral aneurysms, to include treatment for ischemic stroke, carotid artery disease, and neurovascular malformations.
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12803BR
Aliso Viejo, California, USA
310-Direct Manufacturing
Performs the assembly or sub-assembly of medical devices and products in a senior position under limited supervision from line leads and supervisors in accordance with manufacturing documents. Assists the Lead and Supervisor in coordinating production activities. Typical duties: Follow manufacturing instructions to assemble product Record data associated with the building of the product on build records Recognize problems as they arise and interface with Technicians, Engineers or Supervisor to find a solution. Identify continuous improvement opportunities Work with Engineers and Supervisors to perform special assembly requests Assist the Production Lead to address day to day production issues including staffing needs, material availability, and equipment status Follow all related quality, compliance, and company policies and procedures Understand operations objectives and work with team members to achieve overall production goals Responsible for learning and maintaining knowledge and skills to perform majority of the manufacturing processes successfully Train other assemblers on certified manufacturing procedures as directed by the Lead and Supervisor Act as a Production Lead as needed Provide employee performance feedback to Lead and Supervisor Meet all performance standards and metrics by using time and resources efficiently Maintain safe and clean working environment by keeping work area in a neat and organized manner Must be willing to work overtime when needed #LI-DNI -
12798BR
Alajuela, Costa Rica
3223-Supply Chain CR Phase 2
Responsible of receiving, releasing, issuing materials to the warehouse, production, and customers, as well as the data entry into the ERP system. Maintains and inventories receiving, raw materials and finished goods stock • Run all receiving and shipping tasks, physically and input into JDE • Issues materials for Engineering and production work orders. Maintain the clean room covered with material • Data entry of the inventory database • Report shortages of inventory to buyer/planner and Supply Chain Supervisor • Preparation of finished goods to ship to the sterilizer, customer and distribution centers -
12802BR
Aliso Viejo, California, USA
1510-Clinical Research SMI
This internship offers a hands-on opportunity to gain practical experience in the processes that ensure the safety of our medical devices and therapeutic products throughout clinical development. The intern will develop a comprehensive understanding of safety review workflows and contribute to various activities aimed at identifying, reviewing and adjudication of adverse event data. Job Duties 1. Gain working knowledge of safety review workflows including adverse event and technical event review, CEC adjudication and MedDRA coding of adverse events. 2. Assist in the execution and documentation of clinical safety reviews for ongoing studies. 3. Contribute to continuous improvement initiatives for safety review processes and documentation practices. 4. Support the preparation and review of safety documentation (e.g., narratives, source documents for CEC meeting, and review meeting minutes) -
12573BR
Aliso Viejo, California, USA
410-Marketing Admin
Are you interested in working for an organization that is making a difference in people’s lives every day? We’re a medical devices company that develops innovative neuroendovascular technologies for the treatment of vascular disease. We’re a high-growth, customer-focused company with an entrepreneurial spirit producing some of the most reliable and technologically advanced products supported by proven clinical data. Take a closer look at what TERUMO Neuro has to offer. Marketing Intern The Marketing Intern will assist in the development of strategies, programs and tools to support the promotion of current products and the launch of new products to the market. This role acts as key support to the Upstream and Downstream Product Managers in close collaboration with the Marketing Communications and Digital/Analytics Teams, as well as outside vendors. Typical tasks include, but are not limited to: Developing SWOT analysis and strategies to drive product demand Developing positioning and messaging for existing or new products Developing sales tools such as brochures, advertisements and power-point training presentations Assisting with the implementation of product launch planning, ensuring excellent coordination and field communication Utilizing financial models to assess internal and external marketing opportunities -
12785BR
Alajuela, Costa Rica
320-Indirect Manufacturing
Create, maintain, and support different Master Data domains (materials, customers, vendors, BOMs, PIR/SL, QIR, etc.). Work within the Master Data Management Team and other business functions to execute the creation, maintenance, and validation of data across multiple systems. Responsible for using technical tools and best practices to analyze and measure enterprise data quality and develop action plans to ensure the accuracy, completeness, and compliance of our enterprise data with the necessary standards. Assist in driving data governance policies across all business functions and support compliance. Job duties: Process manual or mass requests for master data maintenance across multiple systems in a timely and accurate manner, ensuring policies, procedures, and SOPs are followed. Troubleshoot master data related problems, identify root causes, and implement solutions with minimal or no supervision. In collaboration with other technical and business experts and master data management, define and implement data governance strategy, policies, controls, and programs to ensure master data is accurate, complete, secure, and reliable. Participate in or lead process improvement initiatives related to data and beyond. Contribute to development and documentation of processes with other functional data owners to support ongoing maintenance and data integrity. Work closely with the business and IT experts to ensure alignment of master data rules, standards, and set up. Conduct data validation and reconciliation processes and perform data quality audits around inconsistent or incomplete data, business rule violations, incorrect data, etc. Define data quality metrics and validation rules. Perform data profiling and cleansing techniques to maintain consistent accurate information. Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization. Perform additional duties as assigned. -
12797BR
France
1209 - Italy
The Tender specialist ensures proper management and administration of public tenders related to region. Job duties: Prepare public tender documentation (administrative/technical/economic) in accordance with the tender requirements and send it electronically. Prepare economic offers/quotations in accordance with instructions received from agents/employees, subject to authorization from Sales Director. Manage customer lists. Experience working with customer support: communication with customers through various channels, processing orders and differents requests; keeping records of customer interactions, transactions comments; managing returns and complaints; providing assistance to sales personnel for customer communications product availability and sales. Perform other duties as assigned. -
12800BR
Aliso Viejo, California, USA
420-North America Sales
Deliver technical, clinical, and educational support for all MicroVention (MV) products. Conduct training sessions and provide case support to physicians and hospital staff. Additionally, collaborate with the North American sales team and demonstrate a strong understanding of neurovascular procedures to enhance overall product effectiveness and patient outcomes. Job duties: Provide clinical case support to physicians and hospital support staff for neurovascular procedures using MicroVention products, ensuring adherence to instructions for use and best practices for optimal safety and effectiveness. Facilitate educational and technical trainings for physicians and hospital support staff, focusing on best practices for the initial use of new technologies and ensuring the safe and effective application of all MicroVention products. Collaborate with the North American Sales team to provide optimal technical and clinical support for product evaluations, new physician users, clinical in-services, and educational programs for all MicroVention products. Develop a comprehensive understanding of the appropriate application of all MicroVention products in neurovascular procedures. Support evaluations of new products through education and clinical case support. Complete assigned administrative tasks promptly and thoroughly, including, but not limited to, trunk stock scans, expense reports, and other duties as directed by the clinical leadership team. Ensure the organization and maintenance of relevant files containing anonymized, HIPAA-compliant case images and documents. Communicate frequently and effectively with local and regional Territory Sales Managers to best support business outcomes through strategic collaboration. Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization. Perform other duties and responsibilities as assigned. -
12799BR
Aliso Viejo, California, USA
652-Clinical Admin-Pre Market Operations
The Clinical Data Programmer and Clinical QA Intern will help provide the Terumo Neuro (TN) Clinical Research & Operations (CR&O) Team with high-quality clinical data in various formats inclusive of (but not limited to): data visualization from multiple clinical systems to help develop the Critical to Quality (CtQ) metrics for risk review and make the best mitigation decisions upon based on the high-quality available evidence. Working with TN CR&O, you'll expand your scope, including an introduction to Good Clinical Practice (GCP), hands-on experience in dealing with real medical device clinical data with opportunities to develop dashboards, metrics, and other visualizations. You will primarily be responsible for learning from and working with the guidance of a Clinical Data Manager, Clinical Quality Assurance Manager, and Clinical SAS Programmer team member as to how to plan and execute programming in support of (but not limited to): Collaborate with clinical research personnel to understand the CtQ metrics that need to be tracked Develop intuitive CtQ Reports, Dashboards, and Data Visualizations that represents Quality Tolerance Levels (QTLs) and Key Risk Indicators (KRIs) of Clinical Studies Assist in preparing reports and presentations based on dashboard insights for key stakeholders Ensure accuracy and integrity of data presented in the dashboard Attend clinical study team and cross functional team (CQA and DM) meetings and provide updates on project process -
12794BR
Aliso Viejo, California, USA
420-North America Sales
Promote and sell the Company’s neurovascular products to customers in assigned territory; provide technical support and educate customers in the use of the Company’s products; manage administrative and business relationship between assigned customers and Company. Job duties: Meet or exceed territory sales goals. Develop and execute a comprehensive territory business plan in collaboration with the Regional Sales Manager (RSM) to drive sales growth, market penetration, and account development. Cultivate customer relationships to advance business and sales objectives. Manage account programs (e.g., pricing, consignment inventory, contracts, promotions, etc.) within assigned territory. Conduct in-services, training sessions, and educational programs for physicians, nurses, and other healthcare professionals to ensure proper product understanding, safe usage, and optimal patient outcomes. Work with Marketing, Customer Service and other functional departments to promote and manage business in assigned territory. Attend and participate in business and training meetings as designated to acquire or strengthen skills on new products or sales programs and clinical procedures. Maintain and expand existing product sales; launch new products into assigned customer base. Support training functions and attend trade shows and sales meetings as required. Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization. Perform additional duties and responsibilities as assigned. #LI-DNI -
12783BR
France
432-France
Manage accounts payable functions in assigned region(s). Job duties: Manage end-to-end accounts payable processes for applicable region(s) including invoice processing, payment processing, and vendor management. Review vendor invoices for appropriate documentation and approval. Ensure accuracy and completeness of financial data by reconciling accounts payable transactions and resolving discrepancies in a timely manner. Prepare and review of bank payments. Post bank transactions and perform regular bank reconciliations. Provide support for month-end and year-end close activities, including preparation of journal entries and financial reports. Assist in audits by providing necessary documentation and explanations related to accounts payable transactions. Stay updated on changes in accounting standards, tax laws, and regulatory requirements affecting accounts payable processes in the EMEA region. Collaborate with cross-functional teams to streamline accounts payable processes and implement best practices. Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization. Perform additional duties as assigned. -
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