Provide technical manufacturing support to Engineering

　　Key Responsibilities:

　　• Utilize manufacturing software (e.g., JDE, QMS,PLM) to update documentation in systems

　　• Execute experiments and tests (following protocols) to develop findings for the validation and improvement of equipment and manufacturing processes/methods based on engineering principles; analyze results, make recommendations, and develop reports for Engineering review. Operate a variety of test equipment to assess characteristics of the manufacturing environment

　　• Compile documentation for archives to ensure appropriate documentation for development work, including ECRs, SOPs, drawings, and tooling, for Engineering approval

　　• Consult with Engineers, Technicians, and Assemblers on processes to execute experiments and/or production runs. Support related to equipment investigations, testing, objective evidence of product dispositions and rework support work necessary.

　　• Collaborate with Engineering in the development of training and documentation materials (e.g., work instructions) for production to enable the seamless knowledge transfer of project and manufacturing processes.

　　• Other incidental duties (e.g. occasional photo copying or deliveries)

　　Education and Experience:

　　H.S. Diploma or equivalent 3 years years experience Required or

　　Diploma - Secondary Education in in Mechanical / Industrial / Biomedical / Chemical / Electrical / Manufacturing Engineering Required

　　Additional Skills:

　　• Excellent computer skills required, including experience with MS Office Suite

　　• Ability to read, comprehend, write and speak English, and good communication skills required

　　• Knowledge of Good Manufacturing and Good Documentation Practices supporting a medical device environment

　　• Strict attention to detail

　　• Ability to provide feedback in a professional, direct, and tactful manner

　　• Must be able to work in a team environment and with minimum supervision

　　• Strong analytical and meticulous

　　• 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

　　Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide.

　　For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.