Quality Engineer

About the role

The Quality Engineer will support manufacturing and quality operations at Baxter's Malta site, ensuring compliance with regulatory and quality standards while driving continuous improvement.

Key responsibilities

• Handle quality issues arising during manufacturing and in‑process or finished product testing.
• Support hold processes for non‑conforming raw materials, sub‑assemblies, and finished products.
• Maintain laboratory equipment in a validated state and qualify new equipment.
• Own NCR/CAPA investigations and participate in investigation teams.
• Assist with internal and external audits, and perform internal audits and in‑process assessments.
• Support manufacturing and R&D projects related to product improvement and new product development.

Required profile

• Engineering or Science degree.
• At least 2 years of experience in manufacturing or quality, preferably in a medical device environment.
• Strong communication, problem‑solving, and report‑writing skills.
• Detail‑oriented and adaptable to change.

Required skills

• Proficiency with Microsoft Office tools.
• Familiarity with laboratory equipment and manufacturing processes.
• Knowledge of EN ISO 13485 procedures.