We are SGS – the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our high professional standards and our sustainability approach guarantee you a future-oriented work environment.
Requirements
- Maintenance of the NB 1639 medical device internal quality management system.
- Managing of daily QA tasks: Updating and maintenance of documents under the MDD, MDR and IVDR scheme, Management the IF database, Collaboration on generic scheme documents, Publishing of documents on the SGS website, Bizzmine (Quality Management System); user communication and maintenance.
- Management of complaints, compliance queries and appeals, Management of continual improvement, Management of document control and records, Perform quality assurance check on updated quality management system documents, Release of updated quality management system documents in Bizzmine, Build a good working relationship with the Global Medical Device Certification / Competency / Technical and Clinical Manager(s), and other Global Medical Device Team members, Undertake personal professional development and ensure appropriate training records are updated, Provide technical support to all parts of the business, Maintain a full knowledge and understanding of SGS procedures, regulations, guidance documents (e.g., MDCG) and external approval criteria, Support the development and maintenance of combined scheme documents.
Benefits
- Flexible schedule and hybrid model.
- SGS university and Campus for continuos learning options.
- Multinational environment where you will work with colleagues from multiple continents.
- Benefits platform.
