Quality Systems Specialist - ISO & Compliance

Medtronic plc; Netherlands; On-site; EUR 55,000 - 82,000; Full time

Benefits offered by this job

Flexible Benefits Package

Short-term incentive (MIP)

Job summary

Medtronic plc in Heerlen, Netherlands, seeks a Quality Systems Specialist to embed quality into distribution and warehousing, ensuring ISO 13485:2016 compliance and driving continuous improvement across the supply chain.

You will partner with DC Operations, Supply Chain and Unit Quality teams to assess processes, lead internal audits and Gemba Walks, and strengthen inspection readiness while reducing quality risks to ensure reliable delivery of life-enhancing medical products.

Qualifications

• Bachelor's degree in Quality, Engineering, Life Sciences, Supply Chain, Business, or related field.
• Minimum 2 years of relevant experience in a highly regulated environment (Medical Device / Pharmaceutical / etc.).
• Strong problem-solving and analytical skills with ability to identify root causes and implement solutions.
• Excellent communication and collaboration skills.
• Fluent English; Dutch language skills beneficial.

Responsibilities

• Serve as primary quality contact for processes in local Distribution Centers.
• Partner with process owners to build quality knowledge and drive continuous improvement.
• Manage ISO certification activities (ISO 13485:2016) and ensure compliance with policies.

Skills

Problem-solving

Analytical skills

Communication

Collaboration

English proficiency

Education

Bachelor's degree in Quality/Engineering/Life Sciences/Supply Chain/Business

Tools

ISO 9001 / ISO 13485

CAPA / Nonconformance / Change Control

Job description

Medtronic plc in Heerlen, Netherlands, seeks a Quality Systems Specialist to embed quality into distribution and warehousing, ensuring ISO 13485:2016 compliance and driving continuous improvement across the supply chain.

You will partner with DC Operations, Supply Chain and Unit Quality teams to assess processes, lead internal audits and Gemba Walks, and strengthen inspection readiness while reducing quality risks to ensure reliable delivery of life-enhancing medical products.