Senior IT Technologist

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life As a key member of the Medtronic team, you will play an integral role in advancing healthcare technologies that make a meaningful difference in patients’ lives. This position offers the opportunity to collaborate with talented professionals in a dynamic environment, supporting our mission to alleviate pain, restore health, and extend life. You will contribute to innovative projects, drive impactful solutions, and help shape the future of global healthcare. A Day in the life: We are seeking a senior-level experienced Senior IT Technical Analyst to join our Regulatory Systems team which supports the Regulatory Affairs functions within all operating units and regions. Primary focus will be on the design and configuration of our Regulatory Systems applications, via which we manage Regulatory Submissions, facilitate the review & approval of Promotional Materials, and maintain our Global Labeling Requirements Repository. The ideal candidate will have a strong background in requirements gathering, writing functional specifications as input for configuration and development efforts, is experienced working in a regulated industry in which strict software validation practices apply, and has experience with communicating with business and IT stakeholders on project status on a global level. Responsibilities may include the following and other duties may be assigned. Consult business stakeholders to understand and evaluate current business processes and turn those into system requirements. Writing system functional specifications and support development teams during implementation phase with testing and quality documentation. Deploy new and current systems, processes, and procedures in a cost-effective manner. Configure system settings, plan, and execute unit, system and integration tests and lead cross-functional linked teams to address business or systems enhancements for applications within the Regulatory Affairs domain. Maintain relevant documentation and ensure proper validation documentation is created for all projects according MSCM (Medtronic Systems Compliance Methodology) and ensuring compliance with applicable regulations such as FDA 21CFR, ISO13485 and EU MDR. Ensure that Medtronic's systems and the information on them are protected in accordance with Medtronic's Information Protection Policies and Standards, as well as best Information Protection practices. Required Knowledge and Expertise: Bachelor’s degree in computer science, Information Technology, or related field. Master's degree preferred. 8 years’ experience as an IT Business Analyst, IT Technical Analyst, or software implementation project member with a preferred focus on the MedTech Regulatory industry. In-depth knowledge of industry best practices and terminology related to the Software Validation Life Cycle Methodology. General understanding of the MedTech Regulatory industry. Excellent communication in English as well as collaboration skills, with the ability to work effectively with global cross-functional teams and business stakeholders. Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. This position ... (truncated, view full listing at source)