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Supplier Quality Engineer - CR/616922_1793265102

Supplier Quality Engineer


Sligo
Contract
Negotiable
Quality
CR/616922_1793265102
Supplier Quality Engineer

Supplier Quality Engineer | 12 Month Contract

Location: North of Ireland (Must be based in Ireland)
Onsite Requirement: 5 days per week
Contract Length: 12 Months

A leading healthcare manufacturer is seeking a Supplier Quality Engineer to support quality oversight activities across its third-party manufacturing network. This role will act as the key interface between internal teams and external manufacturing partners, ensuring products are manufactured in compliance with regulatory requirements, quality standards, and business expectations.

This is an excellent opportunity for a quality professional with experience in medical devices, supplier quality, or external manufacturing environments who is looking to contribute to a fast-paced and highly regulated organisation.

Key Responsibilities
  • Act as the primary quality contact for third-party manufacturers and external suppliers.
  • Lead and support investigations into non-conformances, deviations, complaints, and quality-related issues.
  • Drive root cause analysis and CAPA activities to ensure effective resolution of quality events.
  • Monitor supplier performance through quality metrics and key performance indicators.
  • Review and approve quality documentation in line with internal and regulatory requirements.
  • Support change control activities and assess potential quality and compliance impacts.
  • Participate in supplier audits, quality reviews, and regulatory inspections.
  • Identify opportunities for continuous improvement across supplier quality and external manufacturing operations.

Experience & Requirements
  • Proven background in a regulated manufacturing environment, preferably medical devices.
  • Experience working with third party manufacturers, contract manufacturers, or suppliers.
  • Strong understanding of investigations, CAPA, non-conformances, and change control processes.
  • Working knowledge of ISO 13485 and MDR requirements.
  • Excellent communication and stakeholder management skills.
  • Ability to manage multiple priorities and drive projects to completion in a fast paced environment.
  • Must be currently based in Ireland and available to work onsite 5 days per week.

Please get in touch for further information or to discuss your suitability for the role.

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