QA Auditor 2

About the role

The QA Auditor 2 ensures that all incoming materials and components meet the strict quality, safety, and regulatory standards required in a medical‑technology manufacturing environment. You will work closely with suppliers and internal teams to maintain product integrity and support production demand.

Key responsibilities

• Perform visual, graphical and dimensional inspections on incoming materials, verifying certificates of conformance, analysis, and test reports.
• Apply SOPs, SWIs, GMP, and Good Documentation Practice during inspections and documentation.
• Report and investigate quality incidents, non‑conformances, and safety incidents.
• Communicate discrepancies to suppliers, provide feedback, and coordinate material release.
• Handle non‑conforming materials according to the Non‑Conformance Product Handling Procedure.
• Raise Quality Notifications, quarantine defective materials, and support corrective actions.

Required profile

• Commitment to safety, ISO 14001, and environmental responsibility.
• Understanding of GMP, SOP/SWI compliance, and BD Code of Ethics.
• Ability to identify and escalate abnormalities promptly.
• Strong communication skills with internal and external stakeholders.

Required skills

What we offer

• Opportunity to work for a leading global medical‑technology company.
• Engagement in a purpose‑driven environment focused on health innovation.