Quality Engineer III Job Details

Job Description Quality Engineer III Work mode: HybridOnsite Location(s): Propark Free Zone, Coyol de Al, A, CRAdditional Locations: N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, well give you the opportunity to harness all thats 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, well help you in advancing your skills and career. Here, youll be supported in progressing whatever your ambitions. This position provides an exciting opportunity to work for a worldwide and diverse company who puts patients first. The Design Assurance Quality Eng III will provide quality engineering support to products in the Endoscopy division working alongside a high-performing cross functional team, applying problem-solving, critical thinking and risk management skills to ensure product safety and performance. Design Quality Assurance (DQA) acts as the quality representative from a design perspective, responsible for design controls and risk management of products to ensure safety and compliance with internal procedures and regulations. In sustaining, DQA collaborates with multiple functions: R&D, Regulatory Affairs, Marketing, Medical Safety, Operations (Manufacturing, Quality, Production) and others to support initiatives for existing products on the market, such as: design changes, preventive / corrective actions and cost reduction initiatives.Your responsibilities include:Contributing to all aspects of Design Quality Assurance activities in an FDA/EU MDR regulated environment. Working within a cross functional team of Sustaining Engineers and Specialists such as: R&D, Regulatory Affairs, Marketing, Medical Safety, Manufacturing, Quality, Production and others. Supporting the design, development, and test of finished devices and accessories in the Boston Scientific Endoscopy division during their development life cycle, focused on sustaining existing products on the market. Provide quality and compliance input to project teams for project decisions and deliverables (i.e Design Change Analysis, Design Inputs, Design Outputs, Test Methods, Design Reviews, Design V&V, Usability Testing and Labeling). Participate in product, system, and sub-system level design changes with focus on device design evaluation, design controls, product risk mitigation, and other risk management activities. Champion compliance to company policies, work instructions and SOPs. Support the creation, review and maintaining of risk management documentation such as: Hazard Analysis, Task Analysis, Design Failure Mode and Effects Analysis (DFMEA), Fault Tree Analysis (FTA) and Usability Engineering documentation. Applying sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues (i.e 5 Whys Analysis, Is-Is Not Analysis, Cause and Effect Analysis and DMAIC problem solving methodologies). Participating in Value Improvement Projects (VIPs), cost reduction initiatives such as: new suppliers, alternate materials, design changes, etc. Support DQA activities during internal and external audits, as needed. May perform other duties as directed. What were looking for in you: Minimum QualificationsBS in Biomedical, Mechanical Engineering, or related technical discipline. Minimum of 3 years of medical device or related engineering experience. Working knowledge of the FDA, ISO, EUMDR and medical device industry quality requirements associated with product development, design controls, product risk management, usability engineering and medical device software. Strong communication and presentation skills. Strong problem solving and critical thinking skills. Competent with use of Microsoft Office Suite and Minitab statistical analysis software (or equivalent). Ability to collaborate and work in a global team. Position located in Coyol, Costa Rica. Willing / able to travel approximately