Full-Time Medical Devices Project Manager

• Act as the local representative for SGS Notified Body (NB) for the Medical Device Technical Office in the assigned region.
• Coordinate and monitor certification activities in compliance with the procedures and controlled timelines.
• Maintain an overview of ongoing certification processes and customer contract history, acting as the main contact person between clients, auditors, Product Assessors, clinical and final reviewers, and global teams responsible for certification review, technical management, and certification decision.
• Prepare and monitor the Certification Project Plan and follow up on Change Notifications to ensure they progress according to the defined process.
• Review and monitor Incident Notifications submitted by customers, collect additional information when necessary, and provide written justification for proposed decisions by the Notified or Certification Body.
• Track and report MDTLO KPIs and Delivering Office (DO) relationships (monthly reports).
• Monitor and report PM KPIs and collaborate with other Project Managers to ensure effective global PM and resource planning.
• Support Quality or Regulatory teams with the investigation and resolution of complaints and non-conformities as required.
• Collaborate to identify and plan annual business needs, including forecasts for Y+1 and Y+2.

• Coordinate and manage the client’s certification cycle — covering MDR, IVDR, combined standards with ISO 13485, UKCA, and MDSAP — from contract initiation to certification cycle completion.
• Ensure alignment with SGS NB 1639 procedures and timelines across all stages (on-site audits, unannounced audits, technical documentation assessments, final review).
• Participate in project kick-off meetings with the customer and Delivering Office after contract signature to align project scope and timelines.
• Monitor audit scheduling progress in our internal system and ensure Monday.com is updated accordingly.
• Verify that Technical Documentations are uploaded in SharePoint and that all related information (status, links, and dates) is properly completed in Monday.com.
• Monitor and follow up on Change Notifications to ensure they progress in accordance with defined processes and timelines, supporting overall compliance.
• Coordinate Technical Documentation Assessments between the client, Product Assessors, and the Central Pool.
• Generate and review weekly CertIQ reports to track Technical Documentation Assessment progress and update Monday.com.
• Follow up on concessions and non-conformance reports by reviewing reports and coordinating with Delivering Offices to ensure timely resolution.
• Support the Final Review process by completing the certificate.
• Ensure all certification steps are completed and compliant before the certification decision is issued.
• Collaborate with local Delivering Offices and teams to ensure continuous progress of the certification contract

• Co-develop and maintain tools for tracking project progress and KPIs.
• Ensure all project data and KPIs are accurately updated in Monday.com in line with global reporting requirements.
• Support data integrity by ensuring that client information is correctly entered by the D.O and maintained in our internal system
• Generate and analyse reports to support Delivering Offices (DOs) and the PM team in operational and strategic decision-making.
• Monitor KPI performance, provide feedback and improvement suggestions, and support the implementation of corrective actions.
• Collaborate and share best practices with other Project Managers to enhance global consistency and coordination.

• Collect and consolidate MDTLO business development plans, assess their impact on competence and resource requirements, and provide feedback to SGS management.

• Ensure all communication with customers is timely and professional.
• Review and action all customer requests appropriately.
• Follow timelines for contract execution and maintain proactive follow-up throughout the certification process.

• Bachelor's degree in a scientific or technical discipline
• Project Management certification (e.g. PMP, PRINCE2) is an asset
• Knowledge of QMS/Medical Device approval processes is desirable
• Experience in the medical device industry or familiarity with conformity-assessment processes is advantageous
• Previous project management experience, preferably managing multiple projects in parallel
• Demonstrated ability to coordinate complex projects involving multiple stakeholders
• Experience working within structured, procedure-driven environments
• Fluent in English and Portuguese or Spanish (written and spoken)
• Excellent communication, negotiation, and stakeholder management skills
• Analytical mindset with strong IT literacy (Microsoft Office, Teams, Project Management tool
• Ability to develop good working relationships and adapt to change

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