Senior NPI Engineer - Medical Devices Product Launch

CroíValve

Dublin

On-site

EUR 80,000 - 120,000

Full time

14 days+
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Job summary

CroíValve is seeking a Senior NPI Engineer in Dublin to drive product development of a cutting-edge structural heart device through design, verification, clinical trials, validation and regulatory approvals. This full-time role sits in our Dublin office.

You will coordinate manufacturing processes, develop specs, manage cross-functional projects, and ensure GMP compliance while collaborating with contract manufacturers to bring subassemblies to production.

Qualifications

  • BS or MS in mechanical engineering, biomedical engineering, or related disciplines.
  • 5+ years experience in medical devices.
  • Excellent communication, organizational and time management skills.
  • Considerable experience preparing technical documentation.

Responsibilities

  • Co-ordinate day to day production management to meet company build plan objectives.
  • Develop manufacturing processes and provide training to technicians and process operators.
  • Source and implement tooling, instruments and technologies required to manufacture the device.
  • Manage projects to tight timelines with cross functional team alignment and budget management.
  • Develop specifications, process development, training, production instructions, material specifications and procurement.
  • Develop and update documentation relating to equipment or processes to manufacture the device in a controlled manner in line with regulatory standards.
  • Develop and execute DOEs to characterize impact of process parameters on manufacture.
  • Apply risk controls and measurement methods to minimise risk throughout the manufacturing process.
  • Execute process FMEAs, process validations including IQ, test method validation, software validation, OQ and PQ.
  • Work with contract manufacturers to implement production/assembly processes and layouts for subassemblies.
  • Support quality activities for device manufacturing including inspection standards, plans and CAPA/NCR resolutions.
  • Support product builds to ensure product is manufactured in line with specifications.
  • Plan daily activities of operators to achieve production to demand plan and adjust schedules.
  • Support identification and implementation of process improvements (yield, capacity, efficiencies).
  • Develop hands-on understanding of manufacturing procedures, processes and equipment.
  • Ensure GMP compliance in manufacturing areas.
  • Support EHS rules and drive adequate control measures.

Education

B.S. or Masters in mechanical engineering, biomedical engineering or related disciplines
5-10+ years experience in medical devices
Excellent communication, organizational and time management skills
Experience preparing technical documentation

Job description

CroíValve is seeking a Senior NPI Engineer in Dublin to drive product development of a cutting-edge structural heart device through design, verification, clinical trials, validation and regulatory approvals. This full-time role sits in our Dublin office.

You will coordinate manufacturing processes, develop specs, manage cross-functional projects, and ensure GMP compliance while collaborating with contract manufacturers to bring subassemblies to production.

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