MedTech Product Development Engineer: Design & Compliance

Medial Group; Juncos (PR); Presencial; USD 65.000 - 90.000; Jornada completa

Descripción de la vacante

Medial Group in Juncos, Puerto Rico, is seeking a Product Development Engineer to support design, development, and continuous improvement of medical device products. You will implement engineering changes, maintain design documentation, and ensure compliance with quality and regulatory requirements.

The role collaborates with Engineering, Manufacturing, Quality, Planning, and Materials to drive design solutions that improve performance, manufacturability, and efficiency.

Formación

• Minimum of 2 years of engineering experience in product development or manufacturing engineering.
• Experience in regulated industries such as Medical Device, Pharmaceutical, or Life Sciences preferred.
• Experience managing engineering changes and design documentation.

Responsabilidades

• Support product design, development, and engineering change activities throughout the product lifecycle.
• Prepare and maintain engineering documentation, specifications, and technical records in accordance with company quality standards.
• Initiate and process engineering change documentation, including PCH, RCH, DCH, QCH, MCS.
• Collaborate with Product Development, Manufacturing, Quality, Materials, Tooling, and Planning teams to ensure design feasibility and manufacturability.
• Modify existing product designs and components to improve functionality, manufacturing efficiency, and field performance.

Conocimientos

Strong communication

Analytical skills

Problem-solving

Organizational skills

Independent work

Cross-functional collaboration

Leadership coaching

Educación

Bachelor's degree in Mechanical, Biomedical, Industrial Engineering or related field

Advanced degree (preferred)

Herramientas

Agile MAP/PLM

SAP

Design Control Systems

CAD software

Quality Systems

DFM

Descripción del empleo

Medial Group in Juncos, Puerto Rico, is seeking a Product Development Engineer to support design, development, and continuous improvement of medical device products. You will implement engineering changes, maintain design documentation, and ensure compliance with quality and regulatory requirements.

The role collaborates with Engineering, Manufacturing, Quality, Planning, and Materials to drive design solutions that improve performance, manufacturability, and efficiency.