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 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.
At SGS, we have an open corporate and international culture. We offer a dynamic work environment in a leading global company. Our high professional standards and our sustainability approach guarantee you a future-oriented work environment. We invest in our employees for the long term and are committed to supporting your development within the company. Integrity, Health, Safety & Environment, Quality & Professionalism, Respect, Sustainability, and Leadership.
Maintenance of the NB 1639 medical device internal quality management system.
• Managing of daily QA tasks:
~ Management the IF database,
~ Collaboration on generic scheme documents,
~ Bizzmine (Quality Management System); This role will report to the Quality & Regulatory Manager, Business Assurance.
It is remote based, and we are open to candidates located everywhere across Europe. But they must hold a valid work permit for their country of residency.

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
Maintain a full knowledge and understanding of SGS procedures, regulations, guidance
Good working knowledge of quality management systems including CAPA management,
document control and good documentation practices (GDP),
• Ability to organise own workload considering priorities set by the global medical device quality
Ability to adapt quickly and demonstrate flexibility,
• Good working knowledge of the main MS office tools (Word, Excel, Outlook),
• Fluent written and spoken English.
Detailed understanding of global medical device regulations MDR and IVDR, and medical
Knowledge of accreditation standard ISO 17021-1:2015, ISO 13485, ISO 9001.

Experience
Significant work experience in a position with QA responsibility.
Experience working with medical devices,
• Auditing experience against recognised standards.

Bachelor’s degree (or higher) in Biomedical Sciences or similar field (e.g., Medical device training on MDD, MDR, IVDR or ISO 13485
• Medical device auditor
Please send your CV in English

Join a globally recognized and stable company, a leader in the Testing, Inspection, and Certification (TIC) industry.
Enjoy a flexible schedule and work model.
Access SGS University and Campus for continuous learning options.
Thrive in a multinational environment, collaborating with colleagues from multiple continents.
Agevolazioni from our comprehensive benefits platform.
We value diversity and provide endless opportunities to learn, grow your expertise, and fulfill your potential.
Please share your CV in English. The role is fully remote. People from other countries can apply as well.

📌 Quality Assurance Officer (1 year maternity cover) (Milano)
🏢 Sgs
📍 Milano