Associate Engineer

QRC Group

Barceloneta (PR)

Presencial

USD 55.000 - 75.000

Jornada completa

Hace 5 días
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Descripción de la vacante

QRC Group in Barceloneta, Puerto Rico is seeking an Associate Engineer to support quality manufacturing and supplier quality activities. You will set direction for technical tasks within manufacturing disciplines and take ownership of complex projects.

Ideal candidates hold a bachelor’s in Chemical, Industrial, or Mechanical Engineering with 0-2 years of related experience and knowledge of validation, documentation, and process implementation.

Formación

  • Bachelor's degree in Chemical, Industrial or Mechanical Engineering.
  • 0-2 years of experience in Quality Manufacturing or Supplier Quality Engineering.
  • Knowledge with equipment validation, documentation, and process implementation.

Responsabilidades

  • Lead and own complex manufacturing engineering tasks within a discipline.
  • Anticipate issues and recommend solutions where precedent does not exist.
  • Collaborate with peers for task direction and verification activities.

Conocimientos

Equipment validation
Documentation
Process implementation

Educación

Bachelor's in Chemical Engineering

Descripción del empleo

Barceloneta, Puerto Rico | Posted on 10/22/2026

Associate Engineer with knowledge of technical skills and understanding of the business objectives, manufacturing operations and dynamics of the companys environment to take an effective and proactive leadership role in a specific technical manufacturing discipline. Set direction for, lead, and take ownership of complex manufacturing engineering technical tasks tasks that may have multiple inter-coordinating elements. Will be able both to anticipate and identify key issues and make recommendations for resolution where precedent may not exist and creative thinking is required. Resolution may involve the application of new methods and approaches and may require the consideration of impact with other system components. Interaction with peers and mentors on the individuals projects is generally in the context of peer review to confirm the rationale for task approach direction as well as peer review of verification/validation activities.

Requirements
  • Bachelor’s Degree in Chemical, Industrial or Mechanical Engineering
  • 0-2 years of relevant experience in Quality Manufacturing or Supplier Quality Engineering, preferably in medical device industry.
  • Knowledge with equipment validation, documentation, and process implementation.
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