Quality Operator

Abbott Laboratories; Machelen; Sur place; EUR 32 000 - 45 000; Plein temps

Résumé du poste

Abbott Laboratories in Machelen, Belgium, is seeking a Quality Operator for its EMEA Distribution Center. You will perform inspections, handle non-conforming materials, and support distribution activities while maintaining rigorous quality standards.

The role requires at least 2 years in quality/logistics in regulated environments, proficiency with SAP and Microsoft Office, and knowledge of ISO 13485 or ISO 9001. Fluency in Dutch and English is expected, with a hands-on, process-driven mindset.

Qualifications

• At least 2 years in quality, logistics, or regulated environments.
• Familiar with SAP and Microsoft Office.
• Knowledge of ISO 13485 or ISO 9001 is a strong asset.
• Strong documentation accuracy and record-keeping.

Responsabilités

• Perform incoming and in‑process inspections and identify non‑conforming materials.
• Manage returns, quarantine stock, and stop‑ship materials per quality procedures.
• Ensure proper segregation, storage, and labeling of sensitive materials.
• Assist with internal audits and contribute to continuous improvement.
• Review Device History Records (DHR) to ensure compliance.
• Maintain records in SAP and internal systems.

Connaissances

Quality mindset

Attention to detail

Structured

Team player

Formation

High school diploma

Outils

SAP

Microsoft Office

Description du poste

About the Role

Join our EMEA Distribution Center in Machelen and play a key role in ensuring that life-changing medical devices reach patients safely and compliantly.

As a Quality Operator, you’ll work at the heart of operations, supporting quality processes across incoming goods, storage, and distribution activities. This is a hands‑on role ideal for someone who thrives in a structured, regulated environment and is passionate about maintaining the highest quality standards.

What You’ll Be Doing

In this role, you will:

• Perform incoming and in‑process inspections, identifying and handling non‑conforming materials
• Manage returns, quarantine stock, and stop‑ship materials in line with quality procedures
• Ensure proper segregation, storage, and labeling of sensitive materials (e.g. clinical, biohazard, or pending release)
• Support critical distribution activities including labeling, packaging, and product lifecycle controls
• Assist with internal audits and contribute to continuous improvement initiatives
• Review documentation such as Device History Records (DHR) to ensure compliance
• Maintain accurate records in systems (SAP and internal databases)
• Promote a strong quality culture across the distribution center

What We’re Looking For

Experience & Skills

• At least 2 years’ experience in a quality, logistics, or regulated environment (medical devices, pharma, or similar)
• Comfortable working with ERP systems (SAP) and Microsoft Office tools
• Familiarity with quality standards (ISO 13485 or ISO 9001) is a strong asset
• Strong attention to detail and documentation accuracy

Languages

• Fluency in Dutch and English is required
• Any additional European language is a plus

Your Mindset

• Team player with a hands‑on approach
• Structured, process‑driven, and quality‑focused
• Able to work under pressure and meet deadlines
• Autonomous, yet collaborative
• Analytical and solution‑oriented

Education

• Minimum high school diploma or equivalent

Why Join Us?

• Be part of a purpose‑driven organization improving patient lives
• Work in a highly regulated, international environment
• Opportunity to build expertise in medical device quality and distribution
• Collaborative and supportive team culture

Equal Opportunity Statement

We are committed to creating an inclusive environment for all employees and encourage applications from all qualified individuals, regardless of gender, age, disability, sexual orientation, religion, or background.