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Establishment Labs is changing the medical device, breast health, aesthetics and reconstruction industry by designing, developing, and manufacturing an innovative portfolio of advanced medical aesthetic device technologies and wellness solutions. It is currently the world’s fastest-growing women’s health company. Our Femtech solutions are proudly produced at two MDSAP-certified, carbon neutral, LEED Gold certified, state-of-the-art manufacturing facilities in Costa Rica and are approved for sale in more than 85 countries. Since 2018 the company trades on the NASDAQ stock exchange under the ticker symbol ESTA and has a market cap of around $1.8 billion. This is an exciting opportunity to join an innovative international company in hyper-growth as we launch a significant revolution to transform the women´s aesthetics industry.
Job Responsibility
Review, prepare, and update technical documents and protocols related to commercial and new products
Actively participate in the core team: attend meetings, record actions, and follow up
Attend face-to-face sessions with Multidisciplinary teams
Validate data against internal records
Data collection and analysis for technical evidence
Technical writing and generating clear and accurate reports
Update Risk Managment documentation
Participate in Usability evaluations as Formative and Summative
Proposing improvements, contributing ideas, and participating in problem solving with multidisciplinary teams
Digitizing and organizing documentation (version control, digital archiving)
Interest in medical devices, design control, and good regulatory practices
Requirements
Must be pursuing Chemical engineering, Industrial Chemistry, Industrial Production, Biomedical engineering, Mechanical engineering, Materials engineering