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Diversity - Innovation - Caring - General 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.

About the Role

As a member of our Regulatory Affairs team, you will support medical device regulatory activities by coordinating submissions, maintaining accurate regulatory documentation and helping manage product lifecycle activities, including registrations, renewals and changes. You will collaborate with cross-functional teams to gather required documentation, respond to health authority questions and help ensure regulatory activities remain organized, traceable and on schedule.





This role offers an opportunity to contribute to regulatory activities across Andean markets while partnering with teams including Quality, Supply Chain, Marketing and Clinical.

Required qualifications:
- Minimum of 2 years' experience in Regulatory Affairs or the medical device field.
- Bachelor's degree in biomedical engineering, pharmaceutical chemistry (Química Farmacéutica) or a related field; or another degree with demonstrated experience in medical device Regulatory Affairs.
- Experience working with medical device regulatory documentation and product lifecycle activities, including registrations, renewals and changes.
- Strong attention to detail and organizational skills, with the ability to manage multiple priorities.
- Basic functional English proficiency, with the ability to participate in meetings and understand technical documents, including certificates, IFUs, labeling, technical files and emails.

Preferred qualifications:
- Experien

📌 Regulatory Affairs Specialist I | Perú (Lima)
🏢 Boston Scientific Gruppe
📍 Lima