Manufacturing Engineer
Heredia, Heredia, CR
hace 6 días

Manufacturing Engineer


  • Make product and process improvements which are consistent with zero defect level and low product cost by designing, development and implementing manufacturing fixturing and tooling.
  • Perform qualifications of equipment, fixtures, tools, and processes to ensure the proper functionality by executing lab studies, IQ / OQ / PQ and PPQs following GMPs and internal procedures.
  • Perform technical analysis to resolve in an appropriate way and in the shortest possible time problems related to the product or components by conducting testing utilizing DOE methodology and other experimental design tools.
  • Maintain GMP systems, including pre and post production builds, quality assurance procedures, pre-clinical testing programs, stay in compliance and coordination with the Document Control, clinical, and quality assurance functions in order to support company goals, objectives and policies by following GMP, FDA / Medical Device or Pharmaceutical guidelines.
  • Train staff and operational personnel to achieve successful transfers and proper implementation of new processes.
  • Lead the working group, assigned technicians or temporary workers, as required to ensure compliance with objectives.
  • Production Support : must work close to production lines, which uses equipment, tools and fixtures that are intended for the product assembly and can experience wear or damages that can cause increase on scrap, production delays, reworks, and / or documentation generation.
  • Scrap Reduction and PFY Improvement : implement continuous improvement to have production stable, and without reworks or components changes.

  • University degree in any Engineering, Business Administration, or Pharmaceutical production.
  • At least 3 years of experience in the Medical Device or Pharmaceutical Industry. (Preferred)
  • Experience with basic lab practices, instrumentation, tooling and fixturing.
  • Spanish. (Native)
  • Advanced English skills both written and spoken. (Must)
  • Knowledge in Lean Manufacturing and 5S.
  • Knowledge in Good Manufacturing Practices (GMPs).
  • Able to author comprehensive protocols and reports.
  • Able to author and maintain a Laboratory Notebook.
  • Proactive.
  • Open mind and capable to face changes in a positive way.
  • High leadership level. (Desirable)
  • Ability to work under pressure.
  • Ability to perform computerized project scheduling.
  • Passport and US Visa active, and willingness to travel. (Must)
  • Application Period : 19 / 07 / 2021 - 02 / 08 / 2021 Reference Code : 445269 Division : Pharmaceuticals

    Reportar esta oferta

    Thank you for reporting this job!

    Your feedback will help us improve the quality of our services.

    Mi Correo Electrónico
    Al hacer clic en la opción "Continuar", doy mi consentimiento para que neuvoo procese mis datos de conformidad con lo establecido en su Política de privacidad . Puedo darme de baja o retirar mi autorización en cualquier momento.
    Formulario de postulación