Company Description
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. Our business principles include: Integrity, Health, Safety & Environment, Quality & Professionalism, Respect, Sustainability, and Leadership.
Job Description
Main Purpose of Role
Key Accountabilities
The role encompasses a wide range of responsibilities, including but not limited to the following:
Experience
Additional Information
Why SGS?
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. Our business principles include: Integrity, Health, Safety & Environment, Quality & Professionalism, Respect, Sustainability, and Leadership.
Job Description
Main Purpose of Role
- Leading and coordinating the operational delivery of all medical schemes including MDR and IVDR conformity assessment activities under SGS NB 1639.
- This role ensures the effective performance of clinical, audits, technical, and product assessment functions, driving operational excellence, regulatory compliance, and strategic resource management.
- Oversees all technical teams, manages performance, and supports the development of processes, systems, and personnel to meet business and regulatory objectives.
Key Accountabilities
The role encompasses a wide range of responsibilities, including but not limited to the following:
- Lead and manage technical functions: clinical, auditors, products assessors, for all medical schemes, globally.
- Ensure compliance with ISO 13485, MDSAP, UKCA, and EU MDR / EU IVDR requirements throughout assessment lifecycles.
- Ensure the team follows efficient allocation and utilization of technical resources across all conformity assessment activities (in coordination with Commercial & Delivery).
- Operational management of technical certification activities, including resource allocation, technical KPI monitoring, and process improvements.
- Lead training and competence management strategies across technical teams to maintain regulatory and technical expertise.
- Support proactive recruitment, onboarding, and qualification of personnel involved in conformity assessment.
- Drive continuous improvement of technical workflows, IT systems supporting assessment, and quality management processes to enhance efficiency and service quality.
- Act as key interface with regulatory authorities, accreditation bodies, and internal stakeholders to maintain SGS reputation, designations, accreditations and compliance.
- Monitor and respond to regulatory changes, industry trends, and accreditation requirements to ensure proactive adaptation of technical operations.
- Manage and promote impartiality and conflict of interest policies across all teams (including subcontractors), ensuring independence of conformity assessment decisions.
- Ensure compliance with SGS integrity policies, health & safety standards, and confidentiality across technical operations.
- Foster a culture of client focus, integrity, and continuous development within technical teams (while maintaining impartiality and regulatory rigor).
- Collaborate with Commercial & Delivery to harmonize handovers (contract→planning→assessment), align capacity with demand, and support timely service without compromising compliance.
- Provide strategic input into designation maintenance and regulatory engagement, coordinating technical evidence, metrics, and remediation plans as required.
- Commercial/Delivery Touchpoints carried over for completeness (scoped to technical dependencies):
- Provide technical input to commercial business development and bid responses when needed (e.g., feasibility, scope, technical risk, assessor profiles).
- Support budget/KPI visibility for technical operations and contribute to overall performance management.
- Strong understanding of EU MDR, EU IVDR, UKCA, MDSAP, ISO13485 and MDD.
- Proven and solid leadership in managing cross-functional teams in regulated environments.
- Knowledge of conformity assessment procedures and QMS requirements.
- Excellent interpersonal and stakeholder management skills.
- Strong organizational and change management capabilities.
- Strong commercial understanding and appreciation of the TIC industry.
- Experience in resource planning.
- Qualification as Lead Auditor or Product Assessor under EU MDR/EU IVDR.
- Qualification as Final Reviewer and Decision Maker under MDR or IVDR.
- Experience in a Notified Body or equivalent regulatory organization.
Experience
- Minimum 10 years in the medical device or IVD industry, including experience in design, manufacturing, auditing, or technical documentation assessment.
- At least 5 years senior leadership in a Notified Body managing technical employees.
- Minimum 2 years in revenue-focused leadership roles, including full profit and loss (P&L) accountability, budget management, and financial reporting.
- Demonstrated success in P&L role.
- Demonstrated success in leading high-performing teams and driving operational efficiency, with a track record of delivering measurable, positive organizational impact.
- Fluency in English in addition to the local language.
- Given the complex network internal interactions of this role, experience gained within the SGS Group would be an advantage.
- University degree in medicine, engineering, life sciences, or a related field.
Additional Information
Why SGS?
- Global and very stable company, world leader in the TIC (Testing, Inspection and Certification) industry.
- 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.