Intern Regulatory Affairs
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
Role in Regulatory Affairs Team gives the unique opportunity to gain the understanding of product life cycle in Medtech industry as well as to experience variety of regulatory tasks. You will develop your Regulatory skills every day, while working within a collaborative team environment that fosters professional development while focusing on meeting business objectives.
Internship details:
• Start date: February 2025
• Duration: 6 months
• Working time: 30 hours per week
• Work model: remote with possibility to work from office
Responsibilities may include the following and other duties may be assigned:
• Communication with internal & external stakeholders to support registration process
• Preparation & review of submission files
• Tracking submission timelines for Regulatory Affairs in the local databases
• Coordinate translation of the supportive documentation (IFU, Label, Tech files), if applicable
• Provide support & required Regulatory documents to Tender’s Team and/or Distributors
• Administrate execution of Field Corrective Actions
Required knowledge:
• Pursuing a degree in higher education: science, medical studies, healthcare, engineering, IT, Data Analysis
• Good knowledge of MS office (Power Point, Excel, Word, Outlook)
• Fluency in English (B2 or higher) and Ukrainian
• Based in Ukraine
Would be a plus
• General understanding of Regulatory Affairs principles
• Knowledge or experience with Ukraine’s Technical Regulations
• Eager to learn & develop
• Experience in data analysis
Ruslana
Medtronic Перевірена
