Opportunity Description
Diversity - Innovation - Caring - Integral 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.
Responsibilities
- Assist in process optimization projects for the regulatory affairs area (e.g. database maintenance, regulatory controls, automation).
- Support the team in daily operations and technical tasks such as documentation consolidation and Invima dossier assembly.
- Collaborate with multifunctional teams within the framework of joint projects between the regulatory affairs area and other areas.
- Perform data analysis and report findings.
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