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As a Senior SecOps Security Architect, you will play a key role in protecting SGS's global technology landscape by combining security architecture, engineering, operational excellence and technical leadership. You will work across multiple security domains, partnering with infrastructure, cloud, networking and application teams to design, implement and optimize security controls while ensuring our security platforms operate effectively at scale. A key part of the role will be strengthening our Security Information and Event Management (SIEM) capabilities, helping improve security monitoring, log management, detection engineering, alerting and incident investigation across our global environment. This position offers a rare opportunity to combine architecture, project work, technical ownership, automation and operational security in a truly global environment. What You'll Do Security Architecture & Engineering Design and improve enterprise security controls, technical standards and security baselines. Define security requirements for new infrastructure, cloud and application initiatives. Contribute to security architecture decisions, risk mitigation and security-by-design across projects. Security Platform & SIEM Ownership Own and continuously improve key security platforms, including CrowdStrike Falcon / NG SIEM, Netskope, Cisco Umbrella and F5 WAF . Strengthen SIEM capabilities across log ingestion, correlation, alerting, dashboards and security monitoring use cases. Develop and optimize detection rules and integrate security data from endpoint, cloud, identity, network and application environments. Work with SOC teams to improve detection coverage, reduce false positives and enhance overall monitoring effectiveness. Security Operations Support incident response, threat detection, threat hunting and security investigations. Troubleshoot security alerts and contribute to remediation, forensic analysis and root cause investigations. Identify gaps in controls, monitoring or detection capabilities and drive technical improvements. Innovation, Automation & Governance Automate security processes and identify opportunities to improve operational efficiency. Evaluate new cybersecurity technologies and contribute to PoCs and solution assessments. Maintain security documentation, runbooks and operational procedures. Support audit and compliance activities where required. 8+ years of experience in cybersecurity, security engineering, SecOps or a related field. Strong hands-on experience with SIEM , security monitoring and incident response. Experience with security architecture, engineering and enterprise security platforms. Solid knowledge of endpoint, network, cloud and identity security. Experience working in large, complex or international IT environments. Experience with technologies such as CrowdStrike Falcon / NG SIEM, Netskope, Cisco Umbrella, F5 WAF, Palo Alto, Microsoft Sentinel, Splunk, Azure Security or Microsoft 365 Security would be highly valuable. You are hands-on, pragmatic and comfortable working independently while collaborating with global technical teams. Relevant certifications such as CISSP, CCSP, Microsoft Security, CrowdStrike or Palo Alto are beneficial but not essential. 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!

Au sein de l'équipe Certification de Systèmes, nous recherchons un(e) Business Developer expérimenté(e) , passionné(e) par la vente et la relation client, afin d'accompagner le développement de nos activités de certification et d'audit auprès d'une clientèle diversifiée. Vous contribuerez à la promotion de l'ensemble de notre portefeuille de services dans des domaines variés tels que la qualité, l'environnement, la santé-sécurité, l'énergie, la sécurité de l'information, la responsabilité des organisations, ainsi que les nouveaux référentiels répondant aux évolutions réglementaires et aux attentes du marché. Vos missions Piloter la commercialisation de nos offres d'audit, de certification et d'évaluation, de la prospection jusqu'à la contractualisation et au suivi de la satisfaction client. Définir et mettre en œuvre un plan d'actions commerciales ambitieux, en lien avec la direction commerciale et en coordination avec les équipes techniques. Identifier et développer de nouvelles opportunités d'affaires auprès d'entreprises de toutes tailles et de tous secteurs d'activité. Assurer une activité de prospection soutenue afin de conquérir de nouveaux clients et développer le portefeuille existant. Comprendre les enjeux de vos clients et construire avec les équipes SGS des solutions adaptées à leurs besoins de conformité, de performance et de maîtrise des risques. Développer et animer un réseau de partenaires, prescripteurs et acteurs du marché afin de renforcer la visibilité de nos offres. Assurer le suivi de vos opportunités commerciales, de vos indicateurs de performance et de la bonne transmission des dossiers aux équipes opérationnelles. Partager les bonnes pratiques commerciales et contribuer à la dynamique collective de l'équipe Vous possédez une expérience confirmée en développement commercial B2B (minimum 7 à 10 ans), idéalement dans les services, le conseil, la certification, l'audit ou tout autre environnement à forte valeur ajoutée. Une expérience dans les domaines de la certification, de l'évaluation de conformité, des systèmes de management ou des services aux entreprises constitue un atout, sans être indispensable. Vous êtes un(e) vendeur(se) dans l'âme : vous savez identifier, qualifier, développer et conclure des opportunités commerciales complexes avec efficacité et persévérance. Vous avez un véritable tempérament de chasseur , appréciez l'ouverture de nouveaux comptes et savez développer durablement un portefeuille clients. Vous êtes à l'aise pour interagir avec des interlocuteurs de tous niveaux , de l'opérationnel aux décideurs de haut niveau, et savez créer des relations de confiance sur le long terme. Vous comprenez rapidement les enjeux des clients et êtes capable de construire , avec l'appui des équipes techniques, des solutions adaptées à leurs besoins. Vous avez le goût du challenge, du dépassement de vos objectifs et du travail en équipe au sein d'un environnement exigeant et en évolution. Vous êtes capable de partager vos bonnes pratiques commerciales et de contribuer à la montée en compétences de collaborateurs moins expérimentés. Vous êtes autonome, organisé(e), rigoureux(se) et méthodique dans la gestion de votre activité commerciale et de votre pipeline. Vous combinez sens de l'anticipation, pragmatisme, résilience et réactivité face aux opportunités du marché. Vous êtes orienté(e) client, solutions et résultats, avec une forte culture de la performance commerciale. Vous disposez d'excellentes capacités d'analyse et de synthèse vous permettant d'élaborer et d'exécuter des plans de prospection structurés et efficaces. Vous maîtrisez les outils CRM et accordez une importance particulière à la qualité du suivi commercial et à la fiabilité des prévisions de vente. Vous maîtrisez impérativement l'anglai s, à l'écrit comme à l'oral, et êtes capable d'évoluer dans un environnement international en interagissant avec des clients, partenaires et parties prenantes anglophones. Pourquoi rejoindre la team SGS ? SGS est un groupe international avec des perspectives d’évolution variées. Nous favorisons la mobilité et le développement interne de nos collaborateurs. Nous proposons une diversité de métiers dans de nombreux secteurs d’activités où les compétences se complètent pour offrir une expertise de haut niveau à nos clients. Rejoignez une aventure professionnelle et personnelle passionnante au sein d’une organisation dont le succès repose sur l’expertise de ses collaborateurs et sur des valeurs fortes : passion, intégrité, esprit d’entreprise et innovation . Tous nos postes sont ouverts aux personnes en situation de handicap.

As a Senior Microsoft Dynamics Developer , you will play a key role in the design, development, customization, and evolution of SGS’s Dynamics 365 platform and related business applications. You will contribute to solution architecture decisions, ensure high-quality implementations, and promote scalable, secure, and maintainable enterprise solutions. This role requires strong ownership, deep expertise in Microsoft Dynamics 365, a solid end-to-end technical vision, and the ability to proactively enhance our platforms, integrations, and development standards. What You Will Do Design, develop, customize, and maintain solutions within Microsoft Dynamics 365 (Customer Engagement / CRM). Configure and extend Dynamics using plugins, workflows, Power Platform (Power Apps, Power Automate), and custom integrations. Contribute to solution architecture and technical design decisions across the Dynamics ecosystem and integrated applications. Develop and maintain integrations between Dynamics 365 and external systems using APIs, Azure services, and middleware. Improve and maintain CI/CD pipelines, deployment processes, and DevOps practices for Dynamics environments. Optimize and modernize existing Dynamics implementations, reducing technical debt and improving scalability and performance. Ensure system reliability through monitoring, troubleshooting, and continuous improvement. Collaborate closely with business stakeholders, functional consultants, architects, and cross-functional teams in an agile environment. Bachelor’s or Master’s degree in Computer Science, IT, or a related field. 5+ years of experience working with Microsoft Dynamics 365 (CRM and/or ERP) development. Strong experience with C#, .NET, JavaScript, and Dynamics SDK/customization tools. Hands-on experience with Power Platform (Power Apps, Power Automate, Dataverse). Experience with Azure services (Functions, Logic Apps, Service Bus) for integrations. Solid understanding of software architecture, security best practices, and DevOps. Proven experience across the full software development lifecycle (SDLC). Experience with Azure DevOps, Git, and CI/CD pipelines for Dynamics deployments. Fluent in English and comfortable working in a global, multicultural environment. Nice to Have Experience with Dynamics 365 Finance & Operations (D365 F&O) or dual-write integrations. Knowledge of Power BI for reporting and analytics. Experience with legacy Dynamics CRM versions or migrations to Dynamics 365. Familiarity with front-end frameworks (e.g., Angular) for portal or integrated UI development. Microsoft certifications in Dynamics 365 or Power Platform. 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!

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.