Regulatory Information Management Analyst

🔥 14 hours ago

🌐 Slovakia, Colombia – Remote

🇸🇰 Slovakia – Remote 🇨🇴 Colombia – Remote

💵 €28.2k - €42.2k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧐 Business Analyst

👻 Ghost score 0%

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Medtronic

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1949

🏥 Healthcare

🏭 Manufacturing

⚕️ Healthcare Insurance

Healthcare • Manufacturing • Healthcare Insurance

Medtronic is a global leader in healthcare technology solutions, working to address the most complex and challenging medical conditions. With over 95,000 employees in more than 150 countries, the company is focused on accelerating access to healthcare technologies and advancing inclusion, diversity, and equity in healthcare. Medtronic collaborates closely with healthcare professionals to innovate and optimize treatments and therapies, thus inspiring hope and new possibilities for patients worldwide. The company's commitment to healthcare extends to its focus on impactful solutions and sustainable practices.

📋 Description

• Serve as a primary point of contact for internal users of Regulatory Information Management systems, providing support and issue resolution • Create and maintain submission structures, regulatory records, and business data attributes within the RIM environment • Build and manage system templates, including submission assembly templates and related configurations • Perform data entry, data cleansing, and master data governance activities to ensure data accuracy and integrity • Support implementation and sustainment activities associated with the RIM modernization program • Participate in project meetings, providing status updates, identifying risks, and supporting mitigation activities for assigned deliverables • Monitor adherence to RIM standards, procedures, and work instructions to support regulatory compliance requirements • Identify opportunities to improve system processes, data quality, and user experience through continuous improvement initiatives

🎯 Requirements

• Bachelor's degree in Life Sciences, Public Health, Business, or a related discipline and 2+ years of experience supporting Regulatory Information Management systems, Regulatory Affairs processes, or master data management; or Master's degree and 1+ year of relevant experience • Knowledge of the regulatory affairs lifecycle and regulatory submission processes • Experience supporting end users, managing requests, or resolving system-related issues • Proficiency using Microsoft Office applications, including Excel • Demonstrated ability to manage multiple assignments while maintaining accuracy and attention to detail • Experience working in a medical device, pharmaceutical, or life sciences environment and experience with data governance, data quality management, or system implementation projects are nice to have

🏖️ Benefits

• Competitive Salary and flexible Benefits Package • Short-term incentive called the Medtronic Incentive Plan (MIP) • Wide range of benefits, resources, and competitive compensation plans designed to support every career and life stage