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    • Adherence to current health, safety and environmental best practice, ensuring that all work is appropriately risk assessed.
    • Bachelor's Degree in Engineering.
    • Adherence to current health, safety and environmental best practice, ensuring that all work is appropriately risk assessed.
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    • Experience with organizational change management initiatives.
    • Excellent stakeholder management and communication skills.
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    • Knowledge of Medical Device/Combination Product design control activities with integrated risk management deliverables and human factors/usability engineering…
    • Minimum 10–15 years' experience in medical device manufacturing.
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    • Collaborate with peers and management to meet production targets and escalate issues promptly when output schedules are at risk.
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    • Experience leading investigations within a regulated pharmaceutical, biotechnology, or medical device environment.
    • You have experience in medical device industry or pharmaceutical industry including US and international medical device regulatory submissions/approvals.
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    • Effectiveness of planning escalation management and recovery actions.
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    • Strong background in regulated industries such as medical devices, wellness, supplements, cosmetics, or related sectors.
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    • Strong critical path planning and risk management capability.
    • Strong experience in regulated industries (medical device, supplements, cosmetics, or.
    • Conduct & support risk management activities related to development i.e. PHA, DFMEA etc.
    • Minimum 1-5 years industrial experience in developing electromechanical…

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Job Post Details

Process Engineer - medical device: South Dublin (DT18673) - job post

ICDS Recruitment Consultants
South Dublin, County Dublin
Permanent, Full-time

Job details

Job type

  • Permanent
  • Full-time

Location

South Dublin, County Dublin

Full job description

Process Engineer - medical device: South Dublin.

In this role you will support a high-volume, fully automated manufacturing environment, with responsibility for process development, troubleshooting, maintenance, and continuous improvement of production processes and equipment within the assigned area.

Responsibilities:

  • Develop, design, and evaluate equipment and/or processes. Requirement for novel and innovative approaches in relation to fixtures / jig design and scalability.
  • Develop knowledge to become the subject matter expert for assigned processes.
  • Drive process improvements through identification of problem areas/opportunities and collaborate with internal groups and external vendors using Lean / Six Sigma and project management techniques. Assist with Quality Non-conformances, Customer Complaints and CAPA investigations
  • Liaise with external equipment manufacturers / suppliers in terms of equipment / fixture design and manufacture.
  • Manage projects related to product & equipment development
  • Adherence to current health, safety and environmental best practice, ensuring that all work is appropriately risk assessed.
  • Liaise with R&D teams as required, providing design for manufacture input on component / assembly development projects.
  • Provide support to operations, optimising existing processes as needed to ensure that engineering work orders / production related goals are met.

Requirements for this role:

  • Bachelor's Degree in Engineering
  • At least 3 years' process engineering experience within a regulated manufacturing environment
  • Process optimisation with strong background in design of experiments essential.
  • Experience with Cognex or other Vision Systems, pick and place operations, and form fill seal would be desirable.
  • High speed automation experience, test equipment fixture design and documentation is advantageous.

Job Types: Full-time, Permanent

Work Location: In person

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