Manufacturing Engineer 2
hace 10 días

Job Description

In this role, you have the opportunity to

The Manufacturing Engineer sustains manufacturing production floor and / or sterilization and packaging area. Also identify, evaluate, develop, coordinate, validate and implement improvement projects for current processes as well as receiver of product transfers according to the applicable regulations, corporate policies, guidelines and plant procedures.

You are responsible for

Lead multi-functional teams both inside and outside the Costa Rican plant including suppliers of components, services and others.

Provide technical support for the sustaining, design improvement, evaluation and implementation of improvements on current and new production and administrative processes.

This job specification should not be construed to imply that these requirements are the exclusive standards of the position.

Incumbents will follow any other instructions, and perform any other related duties, as may be required by their supervisor.

You are a part of

A leading health technology company with a multinational workforce of approximately 77,000 employees and globally present with sales and services in more than 100 countries worldwide.

To succeed in this role, you should have the following skills and experience.

To succeed in this role, you should have the following skills and experience


  • Bachelor’s degree in Industrial, Mechanical, Chemical, Systems, Electrical, Electronic or Electromechanical Engineer from a recognized University.
  • Preferably at Licenciatura degree for levels I and II, Master s Degree for senior level and above is a plus (or experience demonstrate).

  • Adequate combination of educational background and / or experience in Manufacturing, medical or electronic Companies to effectively perform self-training.

  • Strong knowledge in Spanish and English (Strong oral and written communication skills )
  • Desirable demonstrated knowledge and understanding of GMPs, FDA regulations, Quality System Regulations (QSR), ISO 13485 and ISO 14644-
  • 14698.requirements and Japan regulations.

  • Senior Engineer : more than 5 yrs. Experience in similar positions or 4 yrs. in the Medical Devices or other regulated industry.
  • A minimum of five years related experience and / or training; or equivalent combination of education and experience within a regulated environment.

  • Knowledge of medical devices manufacture or other regulated industries
  • Skilled at building partnerships within the organization and coordinating with support departments. A team player with a positive, customer-oriented attitude.
  • In return, we offer you

    In order to develop your full potential, we will offer you the flexibility, encouragement and opportunities to keep you inspired and engaged.

    After all, working at Philips is more than a job. It is an experience full of amazing moments that will transform you in a lasting and positive way, since together we can improve the world.

    Philips es un empleador que ofrece igualdad de oportunidades. Todos los candidatos calificados recibirán consideración para el empleo sin distinción de raza, color, religión, edad, orientación sexual, identidad de género, nacionalidad, información genética, credo, ciudadanía, discapacidad, veterano protegido o estado civil

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