Engineer I / Technol, Automation (2 Years Contract) - #1133398

Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and discovering lasting solutions for unmet patient needs. Our Engineer I position is a unique career opportunity that could be your next step towards an exciting future.

How you’ll make an impact:

• Perform assigned tasks—including testing, machine issues, CAPA, non-conformances, and audit observations—of simple to moderate complexity.

• Support design, prototyping, assembly, and process or component improvements/automation using established engineering methods and techniques.

• Responsible for the design, analysis, modification, and integration of robotics, automation technologies, and processes related to equipment. Ensure applicability to programs and products, handling complexities ranging from simple to moderate.

• Support and participate in experiments, research, design, configuration, test, modification, fabrication, and assembly of prototypes.

• Provide technical directions to technicians on conducting tests; train technicians and provide feedback; and coordinate technician work.

• Develop training and documentation materials (e.g., work instructions) for automated solution to enable the seamless knowledge transfer of project and manufacturing processes.

• Other incidental duties assigned by seniors/supervisor.

What you’ll need (Required):

• Mechanical design experience with expertise in SolidWorks or similar tools.

• Strong design portfolio demonstrating out-of-the-box thinking and creativity.

What else we look for (Preferred):

• Strong documentation, communication (written and verbal), and interpersonal skills, including consultative and relationship management.

• Solid grasp of engineering principles, theories, and concepts.

• Skilled in problem-solving, organization, analysis, and critical thinking.

• Knowledge of applicable FDA regulations for the medical device industry.

• Strict attention to detail.

• Possesses the ability to interact professionally with all organizational levels.

• Ability to manage competing priorities in a fast paced environment,  including the ability to manage vendors and project stakeholders.

• Effective team player with proven collaboration skills.

• Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control.