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Production Engineer Medical Device Plymouth

Job LocationPlymouth
EducationNot Mentioned
Salary30,000 - 32,000 per annum
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent , full-time

Job Description

Production Engineer (Medical Device) Plymouth, £30,000-£32000A fantastic opportunity for a Production Engineer to join a UK based developer and manufacturer based in Plymouth.Role responsibilities:Responsible for setting up and supporting all manufacturing processes across both a.m. and p.m. shifts, process development and new production introduction to deliver outputs in line with the business objectives on safety, quality, delivery, and cost. Toexecute site support activities and provide maintenance of all relevant operational equipment to ensure longevity and availability.

  • Working closely alongside production operations on alternating shifts to ensure the start-up / shut down and continual running of all manufacturing processes.
  • Establish & maintain standard processes within the validated process window plus optimisation of the technical performance for all manufacturing elements.
  • Investigate and resolve issues related to the technical performance and cost variances
  • Participate with continuous improvement activities.
  • Assist with the introduction of new products and processes into manufacturing
  • Development of new standard processes and ensure optimal implementation into manufacturing supported with initial procedures, training and coaching of manufacturing.
  • Maintain all production equipment to the defined schedule and provide maintenance of the whole site requirements including, fire system testing / training, legionella checks, calibration, and contractor control.
Role requirements:
  • Current experience in production environment support role (or 5 years min).
  • Minimum of HNC level qualification in mechanical, electronic, industrial, or manufacturing engineering, or similar.
  • Experience of developing and/or testing a process within a clean room manufacturing environment.
  • Experience in process and product validation (sterile packaging according to ISO 11607) would be advantageous.
  • Understanding of a quality management system (ISO13485 / FDA) and medical device manufacturing advantageous.
  • Very good MS-Office skills, especially Excel.
  • Strong organizational skills with the ability to communicate at all levels of the organization.
  • Effective time management with the ability to set priorities.
Adecco Lifesciences is acting as an Employment Agency in relation to this vacancy.

Keyskills :
productionmaintenanceengineerprocess

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