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Production Engineer

Polimed Sp. z o.o.

  • Poleczki 12, Warszawa
    Warszawa, Masovian
  • offer expired 2 months ago
  • contract of employment
  • full-time
  • specialist (Mid / Regular)

Polimed Sp. z o.o.

Poleczki 12


Your responsibilities

  • supervision of the production proces, including production in a clean room with a ISO 7 cleanliness class by the instructions determined by Polimed, production and quality processes, and occupational safety rules (To make / have production plans suitable for the short, medium and long term production targets of Polimed, and to ensure their implementation)

  • control of the manufactured elements in accordance with the technical documentation

  • analysis and evaluation of product parameters based on the requirements of standards

  • keeping production documentation

  • managing the production department at a later stage of employment, introducing new employees

  • reporting on the implementation of the production plan

  • active participation in the optimization of production processes, implementation of activities resulting in the optimization of costs related to the production proces

  • to carry out the necessary monitoring and inspections in order to realize the production in full and on time with maximum efficiency and minimum waste, according to the prepared program; to detect deviations from the program and to take corrective measures.

  • to take necessary precautions regarding order, cleaning, workplace and work safety in production areas, to improve existing measures and to ensure that the personnel comply with these rules completely.

  • ensuring that machines, power lines and production equipment are organized in a way that ensures continuous operation.

  • to provide maintenance, repair and improvement of machinery, tools and equipment in production and affiliated maintenance directorates.

  • to determine the measuring instruments and their periods to be calibrated and to act with the Management Representative during the calibration process.

Our requirements

  • Bachelor of Engineering to have knowledge about Quality Management Systems, especially ISO 13485: 2016 Medical devices — Quality management systems

  • independence, accuracy and care for the proper organization of the production plant and high quality of work,

  • commitment to learning about production methods and the specifics of the production plant

  • fluent English


  • ability to track multiple tasks and projects.

  • experience in the production of medical devices and production in clean room

  • knowledge of the Turkish language