Supplier Engineer


Cork
Contract
Negotiable
Research and Development
CR/595083_1780409678
Supplier Engineer

Overview

We are seeking a Supplier Engineer to support supplier-related engineering activities within a medical device environment. This role will focus on material qualification (particularly plastic components), technical supplier management, and supplier change control. The ideal candidate will have a strong engineering foundation, experience working with suppliers, and a solid understanding of quality and validation processes.

This is an opportunity suited to someone with 2-5 years of experience, positioned between junior and senior level, looking to further develop their career in Supplier Engineering.


Key Responsibilities

Supplier Engineering & Technical Management

  • Act as the engineering interface between the company and external suppliers
  • Manage supplier relationships from a technical and engineering perspective
  • Review and interpret engineering drawings and specifications
  • Support supplier selection, onboarding, and performance monitoring

Material & Component Qualification

  • Lead and support material qualification activities, with a focus on plastic parts
  • Ensure materials meet design, regulatory, and quality requirements
  • Work closely with suppliers to ensure compliance with specifications

Supplier Change Management (Core Responsibility)

  • Lead and manage supplier-driven changes from a technical standpoint
  • Assess impact of changes on product quality, performance, and compliance
  • Review supplier documentation, including:
    • Engineering drawings
    • Statistical data and analysis
    • Validation and qualification reports
  • Ensure changes are implemented in line with quality system requirements

Validation & Quality Activities

  • Support and review:
    • Product validation activities
    • Process validation
    • Equipment qualification/validation
  • Apply statistical analysis to evaluate product and process performance
  • Ensure compliance with medical device quality standards and procedures

Data & Analysis

  • Perform and interpret statistical analysis related to supplier performance and product quality
  • Use data to support decision-making and continuous improvement

Skills & Experience

Essential

  • 2-5 years of experience in Supplier Engineering, Quality Engineering, or a related role
  • Experience within medical devices or regulated industries (preferred)
  • Strong ability to read and interpret engineering drawings
  • Knowledge of:
    • Supplier change management processes
    • Quality systems (e.g., ISO 13485 or similar)
    • Validation (process, product, or equipment)
  • Experience with statistical analysis and data interpretation
  • Strong communication skills for supplier interaction

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