MedTronic

  • Northridge, Los Angeles, CA, USA

THE MEDTRONIC MISSION

  1. To contribute to human welfare by application of biomedical engineering in the research, design, manufacture, and sale of instruments or appliances that alleviate pain, restore health, and extend life.
  2. To direct our growth in the areas of biomedical engineering where we display maximum strength and ability; to gather people and facilities that tend to augment these areas; to continuously build on these areas through education and knowledge assimilation; to avoid participation in areas where we cannot make unique and worthy contributions.
  3. To strive without reserve for the greatest possible reliability and qualityin our products; to be the unsurpassed standard of comparison and to be recognized as a company of dedication, honesty, integrity, and service.
  4. To make a fair profiton current operations to meet our obligations, sustain our growth, and reach our goals.
  5. To recognize the personal worth of employees by providing an employment framework that allows personal satisfaction in work accomplished, security, advancement opportunity, and means to share in the company's success. 
  6. To maintain good citizenship as a company.

 

MedTronic Northridge, Los Angeles, CA, USA
Sep 22, 2020
Full time
The  Principal Regulatory Affairs Specialist, International  is responsible for supporting and developing regulatory strategy, preparing global submissions and obtaining approval to introduce Medtronic Diabetes products and therapies to markets worldwide.This role focuses on regulatory support for the international markets outside of the US and EU. In this role, you will have RA responsibility for handling multiple Class I, Class II and Class III products, working within a collaborative team environment that fosters professional development while focusing on meeting business objectives with excellence. A Day In The Life Handle preparation and processing of documentation required for product registration of Medtronic Diabetes products in applicable international markets outside of the US and EU Prepare international submissions for new product introductions, license renewals and product changes in assigned geographies Manage and monitor...
MedTronic Santa Rosa, CA, USA
Sep 22, 2020
Full time
The  Senior Regulatory Affairs Specialist  is responsible for planning and executing global regulatory activities necessary to introduce new Class II and Class III coronary and renal denervation products/ indications to market within the US and International Regions. The Senior Regulatory Affairs Specialist will provide advice and strategic direction for regulatory filings as well as prepare worldwide regulatory submissions including but not limited to original IDEs and PMAs, IDE and PMA Supplements, FDA Pre-Submissions, Shonin applications, Canadian Medical Device License Applications, and EU MDR Design Dossiers. This role works within a cross functional, collaborative team environment that fosters professional development while focusing on meeting business objectives with excellence.This role is an excellent opportunity for the right regulatory professional to take their pre-market regulatory career to the next level at the world’s leading medical device company....
MedTronic Northridge, Los Angeles, CA, USA
Sep 22, 2020
Full time
As the Lead Systems Integrator/Systems Architect, you will be a technical leader for developing Continuous Glucose Monitoring (CGM) solutions for helping people living with diabetes. You will lead the effort to establish the architecture for a technology group, enabling future iteration and feature expansion with a focus on design components for extensibility and reuse. You will accomplish this through working closely with technical teams to understand technology capabilities as they relate to meeting the goals of the business and working closely with business partners to understand future technology/features needed by the market. As a part of the development program, you will establish the trade-off space for a product development program through building consensus amongst business and technical teams regarding scope and feature/performance prioritization. You will work with the technical teams to identify areas of technical risk and ensure that sufficient de-risking activities...
MedTronic Northridge, Los Angeles, CA, USA
Sep 22, 2020
Full time
Principal IT Project Lead –Innovation for Medtronic, Inc. located in Northridge, CA. Responsible for the oversight of IT projects in the innovation portfolio. Coordinates planning, execution and evaluation of IT projects according to timelines, budgets, and project requirements.   Coordinates with cross-functional groups for the business, IT and external vendors. Monitors and reports on product metrics and business KPIs on a weekly basis. Responsible for various Software Application Development projects. Coordinates Business Intelligence, Big Data, Web Based, Mobile, Digital, Ecommerce and Cloud based projects. Responsible for SDLC (Software Development Life Cycle), Agile Scrum,SAFE and Lean Sigma methodologies related projects. Works on IT problem diagnosis using CAPA (Corrective and Preventative Actions), Root Cause Analysis and continuous improvement processes.   Understands the unique IT needs in the Medical Device, Pharma and Life Sciences industry domains....
MedTronic Northridge, Los Angeles, CA, USA
Sep 22, 2020
Full time
In this role as a Senior Quality Engineer – Standards Compliance, you will plan, coordinate, and execute medical device international standards compliance activities to ensure the compliance, safety and reliability of Medtronic Diabetes products throughout the lifecycle of the product (from concept to end of life). You’ll support the development of state of art, Medtronic Diabetes Standards Engineering program and systems for both pre-market and post-market standards related needs and serve as subject matter expert (SME) for the Standards Engineering processes. In these areas, you’ll coach and provide direction to junior Engineers and cross functional teams regarding Standards Engineering processes and best practices.  Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product. Collaborates with engineering and manufacturing functions to ensure relevant and...