Process Technician

JWR Employment Specialists
Published
October 11, 2023
Location
Galway, Ireland
Job Type
Hours of Work
Monday to Thursday
Education Requirements
N/A
Experience Requirements
5 -8 years of medical device production experience is desired
Job Responsibilities
See job description
Job Industry
Healthcare
Salary
Depending on experience
Salary Currency
Euro
Job Order
1234

Description

JWR Employment Specialists are recruiting a Process Technician for a Medical Device manufacturing company located in Galway.

The person in this role will participate in the production / engineering team providing line support and technical support for commercial product and supporting R&D production introduction.

The role will offer an attractive salary and benefits as well as a four day working week!

Duties include;

  • Supports engineering to drive to yield / efficiency improvement projects for production.
  • Conducts feasibility studies to improve yields, balance the line and increase outputs.
  • Executes preventative maintenance for the cleanroom
  • Executes calibration process for the cleanroom
  • Complete equipment qualification.
  • Supports line issues on a daily basis.
  • Makes decisions on accept / reject criteria in production with support from Quality
  • Participate in daily meetings to drive improvement from a yield, output and efficiency perspective
  • Ensure standard times are accurate and achievable for each part.
  • Supports continuous improvement for production

Skills and Qualifications:

  • Previous experience in a similar or exact role desired.
  • 5 -8 years of medical device production experience is desired.
  • Ability to interact with colleagues / suppliers in a professional manner.
  • Proficient communication skills, written and oral.
  • Flexibility, persistence, resourcefulness, a drive to succeed, and an entrepreneurial spirit.
  • SolidWorks 3D CAD proficiency.
  • Familiarity with Design for Manufacturability and Assembly (DFM / DFA) is desired.
  • Experience working within operations / engineering to develop strong manufacturing process instructions and operator training to ensure smooth product transition into the manufacturing environment is desired.
  • Familiarity with FDA QSR and ISO 13485 medical device regulations is desired

 

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