Additional Locations: Costa Rica-Coyol Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At our company, we value diversity and believe it is our greatest strength.
We are committed to empowering women, supporting the LGBTQ+ community, and creating opportunities for individuals with disabilities.
Our belief is that your diversity enriches our work environment.
As an equal opportunity employer, we wholeheartedly welcome applications from all qualified candidates, regardless of their background.
Additionally, we have a Gender Equality Policy that reflects our commitment to fairness and equality in the workplace.
Hybrid Roles: Boston Scientific's hybrid workplace includes Working From Home and onsite.
You will have the opportunity to discuss details in the interview.
About the role Develops new technology, products, materials, processes, or equipment for projects with moderate complexity.
Under limited supervision/guidance, compiles, analyzes, and reports operational, test, and research data to establish performance standards for newly designed or modified products, processes, and materials.
Your responsibilities include: Fully participates in and successfully contributes to project teams typically including the following activities: product design and development, test of materials, preparation of specifications, process capability studies, research investigations (animal and clinical studies), report preparation, and process/test documentation.
Develops solutions to a variety of problems of moderate scope and complexity where analysis of situations or data requires a review of identifiable factors.
Works under general direction regarding the progress of projects and special assignments.
May seek guidance in resolving problems, interpreting established policies, procedures and practices.
Work is reviewed for soundness of judgment.Selects techniques to solve complex problems and make sound design recommendations.
Summarizes, analyzes, and draws conclusions from test results.
Designs and prepares standard reports/documentation to communicate results to technical community.
Performs troubleshooting on new products/process problems as related to design, material, or process.
Cultivates a wide range of internal business relationships and begins to develop an external network of resources to facilitate completion of tasks.
May lead a project team of small to moderate scope.
Influence exerted at peer level and occasionally at first levels of management.
Engages with internal company and external contacts.
Represents organization on specific projects.
Uses diplomacy and tact in interactions and problem solving.
Translates customer needs into product requirements and design specifications.
May train, provide work direction and supervise technicians and entry-level engineers.
Invents/ creates concepts and designs for new products/processes, and submits idea disclosures.
Demonstrates PDP/TDP system knowledge through delivery of high quality and high impact deliverables.
Works cooperatively with process development, quality, manufacturing, regulatory, clinical, and marketing on complex projects to ensure project success.
Interfaces with Physicians/Cath Lab personnel to obtain feedback on concepts and performance of new devices.
Responsible for engineering documentation.
Exercises judgment to determine appropriate action.
Has knowledge of alternatives and an understanding of their impact on the business or technological environment.
Designs and coordinates standard engineering tests and experiments.
Designs, procures, and fabricates tooling and fixtures.
Coordinates, manages, and documents project goals and progress and recommends appropriate revisions.
Assesses the feasibility and soundness of proposed engineering evaluation tests, products or equipment.
Liaison between design team and operations at the manufacturing site Required Qualifications: Bachelor's/Licenciature Degree: Mechatronics, Electronics, Electrical, Mechanical, Materials Science, Biomedical, Industrial, Chemical Engineering or related field.
English level: +90%.
Experience: +2 years in related positions.
Knowledge of ISO 13485, MDR, and FDA medical device requirements, including design controls, product life cycle, validation/verification activities, and process improvement.
Please submit Resume in English Requisition ID: 594045 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life.
Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate.
Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen.
So, choosing a career with Boston Scientific (NYSE: BSX) isn't just business, it's personal.
And if you're a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!
Benefits • Life-Work Integration • Community • Career Growth At Boston Scientific, you will find a collaborative culture driven by a passion for innovation that keeps us connected on the most essential level.
With determination, imagination, and a deep caring for human life, we're solving some of the most important healthcare industry challenges.
Together, we're one global team committed to making a difference in people's lives around the world.
This is a place where you can find a career with meaningful purpose—improving lives through your life's work.