Beschreibung
Our Global Medical Device client is looking for an experienced QA Specialist to help them review their systems and procedures in relation to regulatory requirements for their suppliers. This role will be part of a wider quality improvement project being carried out across all QA workstreams to drive regulatory compliance to an outstanding level.The Supplier QA Specialist will be a member of the project team that is reviewing all QA standards for the suppliers and looking to drive quality, efficiency and communication improvements.
Key Responsibilities:
• Review all quality related documentation and contracts with suppliers and assess for alignment with regulatory requirements.
• Communicate with suppliers to ensure adherence to agreements and renegotiate terms where necessary.
• Carry out supplier audits
Requirements
• University degree. Engineering or Science related discipline preferred or equivalent experience
• Significant experience working in the medical device, pharmaceutical or biotechnology industry
• Extensive experience of working with suppliers and able to demonstrate excellent written and verbal communication skills.
You MUST be Fluent in German and English