**Additional Locations**: N/A **Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance** At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing - whatever your ambitions. **What are we looking for?** **Key Responsibilities** - Support process optimization projects in the Regulatory Affairs area (e.g., database maintenance, regulatory controls, automation) - Assist in daily operations such as documentation consolidation and Invima dossier preparation - Collaborate on cross-functional projects with other departments - Conduct data analysis and prepare findings for reporting - Participate in process mapping to identify optimization and automation opportunities - Attend and contribute to team meetings **Required Qualifications** - Currently pursuing a degree in Biomedical Engineering, Systems Engineering, Pharmaceutical Chemistry, Electronic Engineering, Mathematical Engineering, or a related field - Strong analytical and problem-solving skills - Excellent communication and teamwork abilities - Ability to clearly map and document processes and solutions **Preferred Qualifications (Nice to Have)** - Skills in data cleaning and preprocessing to ensure accuracy and consistency - Interest or experience in programming languages, automation scripts, or database management - Familiarity with regulatory documentation and dossier assembly processes - Interest in regulatory affairs or process improvement initiatives **Requisition ID**:605640