Verified Tech Jobs & Hiring Companies, Updated Every 24 Hours

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.

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!