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NPI Engineer

ID
14537
Location
Leitrim, Ireland
Role Type
Permanent

NPI Engineer

Similar Jobs
NPI Engineer
Location: Leitrim, Ireland 

As an NPI Engineer, you will be at the forefront of innovation, playing a pivotal role in bringing cutting-edge medical devices, particularly catheters, from concept to reality. Your expertise and dedication will directly impact the quality, safety, and success of our clients products. If you are passionate about innovation, quality, and making a difference in healthcare, we invite you to join our clients team and be part of a journey that transforms ideas into life-saving solutions.

Responsibilities:

  • Leading Projects and Project teams to ensure Project Goals are met especially on time delivery, quality requirements and cost targets are achieved.
  • Planning, implementing and co-ordination of New Product Introductions to include: product design, product specifications, process validations identification of training needs, process & equipment lay-out, production procedures, material specifications, material & packaging procurement in accordance with Procedures and Regulatory standards.
  • Ensure the requirements of ISO 13485, ISO 45001, ISO 14001 and ISO 50001 are considered during design, development and new product introduction and integrated into production processes.
  • Sourcing and implementing tooling, equipment and technologies, as required to implement the manufacture of new and existing production. Co-Ordinating the supply of extrusions, if required, with the Extrusion department including agreeing specifications of tubing, resins and quality requirements.
  • Ensuring effective and comprehensive customer communication throughout the duration of the project.
  • Planning and co-ordinating New Product Design to include Design Inputs, Design Outputs, Design Verification and Design Validation including, where necessary, Clinical trials, Technical Files, Technical Reports and Design history Files in accordance with procedures and Regulatory Standards.
  • Development of Manufacturing Process in conjunction with New Product Introduction Team including, as required, training of technicians, process operators and other staff.
  • Planning and implementing manufacturing cell lay-outs, work station design and material handling to ensure efficient manufacturing to meet product cost targets, efficiency targets and quality targets.

Qualifications

  • Third level engineering qualification in Polymer, Biomedical, Mechanical, Design; Minimum Bachelor’s Degree in a Science / Technology / Engineering related discipline (Mechanical, Manufacturing, Automation or equivalent)
  • Ideally 2-3 years experience in new product introduction, manufacturing, quality or process engineering, preferably in catheter manufacturing.
  • Students (unqualified) will be assigned to a fully competent individual. Co-signing will be implemented by the student’s Manager.
  • An Associate position may exist where there is limited experience and will be assigned to an experienced Engineer.
  • Experience in Project Management regarding new product introduction, preferably in a Medical Device environment.
  • Preferably highly competent in manufacturing processes used for manufacturing catheters etc, including extrusion, moulding, balloon forming, braiding, packaging and other assembly techniques.

For further information on this role please contact Hannah Browne +353864409255 or email careers@hero.ie

Check out all our open jobs on our HERO Recruitment website – https://www.hero.ie/

Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.

Data can only be transferred outside of the EEA on the basis of standards contractual clauses, to a country for whom an adequacy decision has been given by the European Commission or where the express permission of the data subject has been given. You have supplied us with your personal data in the process of applying for a position. Our client company may have personnel outside of the EEA who will review you data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.

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