At the Straumann Group , we're on an exciting journey of growth, innovation, and impact – driven by our mission to improve oral health and transform millions of lives worldwide. United by a shared goal, we give our best every day and cultivate a performance-oriented, player-learner culture that fosters collaboration, curiosity, and ambition. As a Supplier Quality Manager (m/f/d) , you will lead our Supplier Quality Management function and play a key role in ensuring compliance, quality, and supplier performance across the global Straumann Group. You will collaborate with internal and external stakeholders worldwide and drive continuous improvement within a highly regulated medical device environment. Supplier Quality Management Managing supplier onboarding, qualification, and monitoring processes Establishing and maintaining Quality Assurance Agreements with suppliers, subsidiaries, and distributors Monitoring supplier performance through KPIs and continuous improvement initiatives Leading and developing the Supplier Quality Management team Quality Systems & Supplier Performance Investigating, reviewing, and approving supplier-related NCRs and CAPAs Supporting supplier qualification activities and ensuring compliance with regulatory and quality requirements Collecting, analyzing, and reporting supplier quality data and KPIs to management Supplier Audits & Compliance Managing the global supplier audit program and audit schedule Planning, coordinating,



and conducting supplier quality audits as lead auditor Training and supporting internal auditors as part of continuous education activities Incoming Inspection & Digital Process Ownership Defining and maintaining incoming inspection plans for the Basel warehouse Performing batch release activities based on quality certificates and documentation reviews Acting as Business Process Owner for supplier document management tools, including Product City lifecycle modules Defining user requirements, ensuring documentation, and coordinating user training University degree in Quality Management, Engineering, Life Sciences, Pharmacy, Medicine, Law or a comparable discipline Proven and strong professional experience in Quality Management, preferably within the medical device industry or pharma Proven experience in Supplier Quality Management and supplier qualification processes Strong knowledge of ISO 13485, MDR 2017/745, MDD 93/42/EEC, FDA 21 CFR 820 (QMSR), and related quality systems ISO 13485 Auditor Training, Lead Auditor certification is an advantage Strong knowledge of SAP, e-QMS systems, MS Office, and document control systems Lean Management Experience Fluent English skills, any additional languages are an advantage You combine strong analytical thinking with excellent organizational skills You are passionate about quality, compliance, and continuous improvement You have experience leading teams and developing talent in a general environment

📌 Quality Assurance Officer (España)
🏢 Institut Straumann
📍 España