Careers at SGS

Main Purpose of Role: • 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. 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. Key Accountabilities: • 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. Skills & Knowledge Essential: • Good working knowledge of quality management systems including CAPA management, document control and good documentation practices (GDP), • Detail oriented, • Strong organisational skills, • Ability to organise own workload considering priorities set by the global medical device quality manager, • Ability to adapt quickly and demonstrate flexibility, • Ability to work in a team, • Ability to write clear procedures, • Good working knowledge of the main MS office tools (Word, Excel, Outlook), • Fluent written and spoken English. A nice to have: • Detailed understanding of global medical device regulations MDR and IVDR, and medical device directive MDD, • Knowledge of accreditation standard ISO 17021-1:2015, ISO 13485, ISO 9001. Experience Essential: • Significant work experience in a position with QA responsibility. A nice to have: • Experience working with medical devices, • Auditing experience against recognised standards. Qualifications Essential: • Bachelor’s degree (or higher) in Biomedical Sciences or similar field (e.g., pharmacy, bioengineering, nurse, or similar) A nice to have: • Medical device training on MDD, MDR, IVDR or ISO 13485 • Medical device auditor Performance Indicators: • Turnaround time for compliance issues/complaints/ appeals, • Efficient running of QMS and release of quality management documents. Please send your CV in English Why SGS? 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. Benefit from our comprehensive benefits platform. Join Us: At SGS, we are dedicated to fostering an open, friendly, and supportive culture that thrives on teamwork. 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.

Main Purpose of Role: • 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. 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. Key Accountabilities: • 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. Skills & Knowledge Essential: • Good working knowledge of quality management systems including CAPA management, document control and good documentation practices (GDP), • Detail oriented, • Strong organisational skills, • Ability to organise own workload considering priorities set by the global medical device quality manager, • Ability to adapt quickly and demonstrate flexibility, • Ability to work in a team, • Ability to write clear procedures, • Good working knowledge of the main MS office tools (Word, Excel, Outlook), • Fluent written and spoken English. A nice to have: • Detailed understanding of global medical device regulations MDR and IVDR, and medical device directive MDD, • Knowledge of accreditation standard ISO 17021-1:2015, ISO 13485, ISO 9001. Experience Essential: • Significant work experience in a position with QA responsibility. A nice to have: • Experience working with medical devices, • Auditing experience against recognised standards. Qualifications Essential: • Bachelor’s degree (or higher) in Biomedical Sciences or similar field (e.g., pharmacy, bioengineering, nurse, or similar) A nice to have: • Medical device training on MDD, MDR, IVDR or ISO 13485 • Medical device auditor Performance Indicators: • Turnaround time for compliance issues/complaints/ appeals, • Efficient running of QMS and release of quality management documents. Please send your CV in English Why SGS? 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. Benefit from our comprehensive benefits platform. Join Us: At SGS, we are dedicated to fostering an open, friendly, and supportive culture that thrives on teamwork. 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.

Main Purpose of Role: • 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. 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. Key Accountabilities: • 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. Skills & Knowledge Essential: • Good working knowledge of quality management systems including CAPA management, document control and good documentation practices (GDP), • Detail oriented, • Strong organisational skills, • Ability to organise own workload considering priorities set by the global medical device quality manager, • Ability to adapt quickly and demonstrate flexibility, • Ability to work in a team, • Ability to write clear procedures, • Good working knowledge of the main MS office tools (Word, Excel, Outlook), • Fluent written and spoken English. A nice to have: • Detailed understanding of global medical device regulations MDR and IVDR, and medical device directive MDD, • Knowledge of accreditation standard ISO 17021-1:2015, ISO 13485, ISO 9001. Experience Essential: • Significant work experience in a position with QA responsibility. A nice to have: • Experience working with medical devices, • Auditing experience against recognised standards. Qualifications Essential: • Bachelor’s degree (or higher) in Biomedical Sciences or similar field (e.g., pharmacy, bioengineering, nurse, or similar) A nice to have: • Medical device training on MDD, MDR, IVDR or ISO 13485 • Medical device auditor Performance Indicators: • Turnaround time for compliance issues/complaints/ appeals, • Efficient running of QMS and release of quality management documents. Please send your CV in English Why SGS? 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. Benefit from our comprehensive benefits platform. Join Us: At SGS, we are dedicated to fostering an open, friendly, and supportive culture that thrives on teamwork. 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.

Main Purpose of Role: • 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. 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. Key Accountabilities: • 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. Skills & Knowledge Essential: • Good working knowledge of quality management systems including CAPA management, document control and good documentation practices (GDP), • Detail oriented, • Strong organisational skills, • Ability to organise own workload considering priorities set by the global medical device quality manager, • Ability to adapt quickly and demonstrate flexibility, • Ability to work in a team, • Ability to write clear procedures, • Good working knowledge of the main MS office tools (Word, Excel, Outlook), • Fluent written and spoken English. A nice to have: • Detailed understanding of global medical device regulations MDR and IVDR, and medical device directive MDD, • Knowledge of accreditation standard ISO 17021-1:2015, ISO 13485, ISO 9001. Experience Essential: • Significant work experience in a position with QA responsibility. A nice to have: • Experience working with medical devices, • Auditing experience against recognised standards. Qualifications Essential: • Bachelor’s degree (or higher) in Biomedical Sciences or similar field (e.g., pharmacy, bioengineering, nurse, or similar) A nice to have: • Medical device training on MDD, MDR, IVDR or ISO 13485 • Medical device auditor Performance Indicators: • Turnaround time for compliance issues/complaints/ appeals, • Efficient running of QMS and release of quality management documents. Please send your CV in English Why SGS? 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. Benefit from our comprehensive benefits platform. Join Us: At SGS, we are dedicated to fostering an open, friendly, and supportive culture that thrives on teamwork. 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.

Main Purpose of Role: • 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. 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. Key Accountabilities: • 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. Skills & Knowledge Essential: • Good working knowledge of quality management systems including CAPA management, document control and good documentation practices (GDP), • Detail oriented, • Strong organisational skills, • Ability to organise own workload considering priorities set by the global medical device quality manager, • Ability to adapt quickly and demonstrate flexibility, • Ability to work in a team, • Ability to write clear procedures, • Good working knowledge of the main MS office tools (Word, Excel, Outlook), • Fluent written and spoken English. A nice to have: • Detailed understanding of global medical device regulations MDR and IVDR, and medical device directive MDD, • Knowledge of accreditation standard ISO 17021-1:2015, ISO 13485, ISO 9001. Experience Essential: • Significant work experience in a position with QA responsibility. A nice to have: • Experience working with medical devices, • Auditing experience against recognised standards. Qualifications Essential: • Bachelor’s degree (or higher) in Biomedical Sciences or similar field (e.g., pharmacy, bioengineering, nurse, or similar) A nice to have: • Medical device training on MDD, MDR, IVDR or ISO 13485 • Medical device auditor Performance Indicators: • Turnaround time for compliance issues/complaints/ appeals, • Efficient running of QMS and release of quality management documents. Please send your CV in English Why SGS? 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. Benefit from our comprehensive benefits platform. Join Us: At SGS, we are dedicated to fostering an open, friendly, and supportive culture that thrives on teamwork. 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.

Primary Responsibilities Lead the definition , validation , and implementation of all architectural choices for Cloud & Software Architecture (SWA) initiatives across the group. Design and oversee cloud‑native application architecture using a holistic , enterprise‑scale approach. Ensure the technical quality , scalability , performance , and maintainability of all solutions delivered by the Software Architecture team . Drive the evolution of existing software architectures and frameworks toward modern technologies, with a strong emphasis on AI‑driven development and GenAI-assisted coding . Manage , mentor, and develop the Software Architecture team . Specific Responsibilities Act as the key technical advisor to the Head of Architecture & Technology on all Cloud & SWA projects . Define the technologies , frameworks , and tools to be used across SWA initiatives. Establish and maintain development standards , architectural principles , and best practices for application design and coding. Oversee the technical implementation of applications and provide hands‑on support to teams when required. Contribute to the design , development , and deployment of SWA applications. Periodically review technical processes and procedures , identifying opportunities for improvement. Lead the technical evolution of applications to maintain performance , stability , and business alignment. Provide 3rd‑level support for live applications. Ensure compliance with the SGS Code of Integrity and Professional Conduct . Education & Experience Master’s degree or equivalent in Computer Science or a related field. 10+ years of experience in software architecture , cloud architecture , and enterprise software development. Experience working in an international and multicultural environment. Fluent in English . Required Technical Skills Strong knowledge of Agile methodologies (Agile, Scrum ). Expertise in XML and web services ( REST , SOAP ). Advanced proficiency in C# and ASP.NET 4.5 . Strong experience with Entity Framework . Advanced JavaScript skills, particularly jQuery . Strong command of SQL Server and SQL . In‑depth knowledge of Microsoft Azure cloud architecture and services. Experience with GenAI‑based coding and AI‑assisted development . Required Soft Skills Strong leadership . Effective people management skills. Excellent communication abilities. Team‑oriented and collaborative mindset. Highly organized , structured , and analytical . Autonomous , proactive, and delivery‑focused . Preferred Technical Skills Good understanding of Web API . Good understanding of WPF . Why SGS? Join a globally recognized and stable company, a leader in the Testing, Inspection, and Certification (TIC) industry. Enjoy a flexible schedule and hybrid work model Access continuous learning opportunities through SGS University and Campus. Collaborate in a multinational environment with colleagues from various continents. Benefit from a comprehensive benefits platform. Apply Now : At SGS, we are committed to fostering an open, friendly, and supportive culture that thrives on teamwork. We value diversity and provide endless opportunities to learn, grow your expertise, and fulfill your potential. Apply now to join our motivated and dynamic team!

Brinda apoyo de ofimática y dibujo CAD para la carga, verificación y modificación de información en el software de gestión de integridad Ultrapipe/PSAIM. Técnico o Profesional de carrera afín a los trabajos a ejecutar 2 años de experiencia en trabajos similares Se solicitara certificado de titulo si corresponde y verificación de recomendaciones.

Realiza la carga de datos, la verificación del cumplimiento de rutas y el seguimiento de indicadores KPI mediante PowerBI para el equipo de Rotatorios. Técnico o Profesional de carreras del sector Industrial o afín 2 años de experiencia en trabajos similares Se solicitara certificado de titulo si corresponde y verificación de recomendaciones.

SGS Fulcrum is seeking an experienced and motivated Robotics Operator to lead the safe and effective delivery of innovative inspection, survey, and monitoring projects across industrial and environmental sectors. This is an exciting opportunity for a technically skilled robotics professional who enjoys field operations, client engagement, and working with cutting-edge technologies. You will play a key role in delivering projects using our fleet of UAVs, ROVs, and UGVs, while supporting project planning, mentoring team members, and driving continuous improvement across robotics operations. What You'll Be Doing Operating and leading the deployment of advanced UAV, ROV, and UGV technologies. Delivering inspection, survey, and monitoring projects safely, efficiently, and to a high standard. Mentoring team members and supporting operational excellence across robotics services. Processing spatial data and producing GIS, mapping, and 3D modelling deliverables. Working closely with clients to provide innovative, technology-driven solutions. Driving continuous improvement in robotics operations, data workflows, and project delivery. Promoting a strong commitment to safety, compliance, and quality in everything you do. We’d love to hear from candidates across Australia! If you’re based in QLD or another state and are interested in joining our team, please indicate your preferred state/location when applying. About You You are a hands-on technical professional with a passion for robotics and a commitment to safety, quality, and client satisfaction. Essential Requirements CASA Remote Pilot Licence (RePL). Experience operating UAVs, ROVs, and/or UGVs within industrial, infrastructure, environmental, or resource sectors. Demonstrated leadership experience in field operations or project delivery environments. Strong understanding of robotics platforms, sensors, and inspection technologies. Knowledge of CASA regulations, WHS requirements, and operational risk management. Experience with GIS and spatial data processing software such as ArcGIS, QGIS, Pix4D, or Agisoft Metashape. Current Australian Driver's Licence. Desirable Experience in asset inspection, environmental monitoring, surveying, or industrial services. Strong report-writing and client-facing communication skills. Experience leading multiple projects and field teams. WHY WORK FOR SGS? Working at SGS means joining an innovative, Global company. Here are some of the benefits to working for SGS. • As a company, we have embraced the shift to flexible work • Sustainability is embedded in our culture and the way we do business • Paid parental leave • Paid time for volunteering day and blood donations • Corporate health & wellbeing offers • Ongoing learning & development • Career development opportunities (Nationally and Globally) • SGS Rewards: Our employee benefits platform with access to retail and online discounts and cashback COME TO WORK AND BE 100% YOU SGS Australia supports a diverse workforce, we encourage applications from people of all ages, nationalities, abilities, and cultures – including Aboriginal and Torres Strait Islander peoples, the LGBTQI+ community and people living with disability. Providing employment opportunities for Aboriginal and Torres Strait Islander people is an important part of our SGS Reconciliation Action Plan (RAP). We truly believe the diversity among us will continue to foster a strong, innovative, and forward-thinking workplace. SGS Australia acknowledges and pays respect to the past, present and future Traditional Custodians and Elders of this nation and the continuation of cultural, spiritual, and educational practices of Aboriginal and Torres Strait Islander peoples.

As part of the Architecture, Intelligence & Technology (AI&T) team , this role plays a key part in shaping and delivering Finance transformation initiatives through the development of innovative digital and AI-driven solutions. The Senior Full Stack & AI Engineer will contribute to the configuration and delivery of a newly established squad focused on Finance transformation, supporting the modernization of processes and ways of working across the Global Finance function. This is a hands-on technical role responsible for the end-to-end development of applications and AI-enabled solutions, including front-end, backend, cloud, DevOps, and AI/LLM integrations. The role will work closely with business stakeholders, architects, and cross-functional teams to deliver scalable, secure, and business-aligned technology solutions. Responsibilities Develop full stack applications using .NET / Python and React, Vue, or Angular Design, develop, and integrate REST APIs Develop and support AI/LLM-based solutions using Azure OpenAI, AI Foundry, and related technologies Implement Retrieval-Augmented Generation (RAG) solutions and vector-based search capabilities Build document ingestion and vector indexing pipelines Utilize OCR and Document Intelligence technologies for document processing automation Manage CI/CD pipelines, deployments, and DevOps activities Collaborate with architects, product owners, and business stakeholders to define technical solutions Ensure solution scalability, maintainability, security, and performance Support agile delivery practices and continuous improvement initiatives Contribute to technical design discussions and problem-solving activities within the squad Provide ongoing support, maintenance, monitoring, and enhancement of AI-enabled business applications in production environments Contribute to identity and governance-related solutions leveraging Microsoft Entra ID and related technologies 5+ years of experience in full-stack software engineering and cloud technologies 1–2 years of hands-on experience with LLM/RAG solutions and AI-enabled applications Proven experience delivering end-to-end technical solutions across front-end, backend, cloud, and DevOps environments Experience working within agile delivery environments and cross-functional global teams Strong communication and stakeholder engagement skills Focused on delivering high-quality user experiences and business value Fluent in English, with the ability to operate effectively in multicultural environments Required Skills: Full stack development ( C#, .NET, Python, React, TypeScript, Vue, Angular ) REST API design and integration Azure Web Apps, Azure SQL, and Microsoft Entra ID Cloud platforms and DevOps practices Azure DevOps, CI/CD pipeline management and deployments LLM/RAG solution development Azure OpenAI and AI Foundry OCR and Document Intelligence technologies Vector indexing and document ingestion Agile methodologies and collaborative delivery Problem-solving and analytical thinking Stakeholder communication and cross-functional collaboration Why SGS? Join a globally recognized and stable company, a leader in the Testing, Inspection, and Certification (TIC) industry. Enjoy a flexible schedule and a hybrid work model. Access continuous learning opportunities through SGS University and Campus. Collaborate in a multinational environment with colleagues from various continents. Apply Now : At SGS, we are committed to fostering an open, friendly, and supportive culture that thrives on teamwork. We value diversity and provide endless opportunities to learn, grow your expertise, and fulfill your potential. Apply now to join our motivated and dynamic team!