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Engr I, R&D, BD Advanced Patient Monitoring

Type

Full time

Location
Dominican Republic-Nave 25-Merengue
Job reference

Req-39211

Posted for

1 month ago

The Sustaining R&D Laboratory provides support for Sustaining / GSC-related projects, and NPD projects for Design verification/validation and feasibilities testing. 
We are responsible for maintaining and improving the product design of DR APM legacy products including new product development, while following design control system guidance. This position is based at Haina as a satellite location since it reports directly to Corporate.

Key Responsibilities:
• Develops, author and execute D&D plans, Design Verification, Design Validations and technical summaries for product design changes following the design control system. Performs DRD assessments for CTQ identification as part of this process.
• Proactively performs (leads) or participates in small (in complexity and technical depth) product design changes to DR legacy products to improve design for manufacturability, product cost, product quality, product testing and for business continuity purposes (DFX).
• Supports day to day requests/activities requiring R&D assessments and approvals from the DR Plant mainly traduced in ECRs, technical summaries and protocols. Reviews and approves process improvements and process changes by means of the change control process to ensure design intent is maintained (Design Control Engineering- DCE).
• Primary contact for basic questions related to product Engineering Specifications, Design Outputs, Product Design & Product Use of DR CC legacy products.
• Supports small (in complexity and technical depth) Value Improvement Projects (Cost Savings and Value Engineering) and Material Projects (Business Continuity). Validates like for like (functional) design changes.
• Analyzes data and interprets standard practices and procedures to establish recommendations for problem solving. Develops solutions to routine problem.
• Supports product stewardship, RA issues of legacy products and work on remediation projects, transfer knowledge in design control system, product use and design and overall technical knowledge. May be required to explain outcomes to and/or keep others who are performing related work informed. Perform other complementary and related duties.

Education and Experience:
Bachelor's Degree in in Engineering (Electrical, Electronic, Mechatronic, Chemical, Biomedical, Mechanical), Product Design or related Engineering discipline no experience Required

Additional Skills:
• Basic knowledge of JD Edwards.
• Basic knowledge of GD & T (Geometric Dimensions & Tolerances) and a tolerance analysis.
• Basic knowledge in computer assisted design tools (AutoCAD, SolidWorks, ProE, etc).
• Basic process and product knowledge.
• Basic knowledge of Statistics (Yellow or Green Belt Certified)
• Knowledge in cGMP Manufacturing Environmental within Medical Device Industry, including knowledge of FDA / TUV guidelines and quality system regulations in general.
• Good computer skills in the use of MS Office Suite
• Basic documentation, communication (both written and verbal) and interpersonal relationship skills
• Basic knowledge of statistical techniques
• Good understanding and knowledge of principles, theories and concepts relevant to Engineering.
• Good problem solving, organizational, analytical and critical thinking skills
• Good knowledge of the processes and equipment used in the assigned work
• Strict attention to detail
• Ability to interact professionally with all organizational levels
• Ability to manage competitive priorities in a fast-paced environment
• Ability to work in a team environment, including the ability to manage suppliers and project stakeholders
• Ability to build productive internal / external productive relationships
• Ability to apply company policies and procedures to resolve issues related to products/processes within an assigned team or work group.
• Ability to comply with the standards, regulations, procedures and quality manuals applicable to Edwards Lifesciences
• 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

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Job reference

Req-39211

Aplicar ahora
Type

Full time

Location
Dominican Republic-Nave 25-Merengue
Posted for

1 month ago


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Aplicar ahora
About Edwards Lifesciences

Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. Through breakthrough technologies, world-class evidence and partnerships with clinicians and healthcare stakeholders, our employees are inspired by our patient-focused culture to deliver life-changing innovations to those who need them most.


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Edwards se compromete a cumplir con los requisitos y orientaciones de nuestras autoridades gubernamentales y a proteger a nuestros pacientes vulnerables y a los proveedores de atención sanitaria que los tratan en todo el mundo. Como tal, todos los puestos de trabajo que interactúan con la atención sanitaria requieren la vacunación COVID-19, lo que incluye a cualquier persona que interactúe directamente con los pacientes y a aquellos que interactúan con los proveedores de atención sanitaria como parte de su función. En caso de ser contratado, como condición para el empleo, se le pedirá que presente una prueba de que se ha vacunado completamente contra la COVID-19 o que tiene una exención religiosa o médica válida para no vacunarse. Este requisito de vacunación no se aplica en los países en los que está prohibido por ley imponer la vacunación. En los países en los que las vacunas están menos disponibles, o en los que existen otros requisitos, podemos instituir medidas alternativas que optimicen la seguridad del paciente y del personal sanitario, que pueden incluir pruebas periódicas de COVID o requisitos específicos de enmascaramiento.

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