Conduct information security management system audits for various standards across Poland and internationally. Prepare post-audit documentation in English and participate in product development, training, and market implementation.
Conduct information security management system audits for clients across Poland and internationally. Prepare post-audit documentation and contribute to product development, testing, and training delivery.
The Global Technical Manager provides senior technical and accreditation leadership for the Business Assurance Certification business. The role sets, maintains, and enforces the global technical framework, accreditation strategy, and governance controls to ensure consistent and compliant service delivery.
Manage remote client engagement and application processing for PCA/PVoC services while ensuring documentation compliance. Coordinate between clients, inspection teams, and laboratories to drive timely issuance of Certificates of Conformity.
Conduct safety assessments and certification audits for industrial machinery and semiconductor manufacturing equipment based on international standards. Provide technical training and seminars regarding product safety regulations and risk assessment interpretations.
Perform third-party audits of medical device quality systems to ensure compliance with ISO 13485, MDSAP, MDD, and MDR standards. Evaluate audit evidence to provide professional recommendations regarding certification and maintain all necessary audit credentials.
Perform third-party medical device audits to ensure compliance with ISO 13485, MDSAP, MDD, and MDR standards. Analyze audit evidence to provide recommendations for certification and manage the audit process effectively.
The Lead Certification Auditor performs third-party audits to ensure compliance with industry standards and regulatory requirements for the pharmaceutical, cosmetics, and personal care sectors. They are responsible for making certification recommendations, managing audit teams, and ensuring all activities align with SGS global and local procedures.
The Lead Certification Auditor performs third-party audits to ensure compliance with industry standards and regulatory requirements for pharma, cosmetics, and medical devices. They are responsible for making certification recommendations, managing audit teams, and resolving issues throughout the audit process.
The Lead Certification Auditor performs third-party audits to ensure compliance with industry standards and regulatory requirements for pharma, cosmetics, and medical devices. They are responsible for making certification recommendations, managing audit teams, and maintaining SGS certification system integrity.
Perform third-party medical device audits to ensure compliance with ISO 13485, MDSAP, MDD, and MDR standards. Analyze audit evidence to provide recommendations for certification and manage the audit process effectively.
Conduct safety assessments and inspections for industrial machinery and semiconductor manufacturing equipment based on international standards. Provide technical training and seminars regarding product safety regulations and risk assessment.
The Operations Planner is responsible for optimizing audit and training event schedules while assigning qualified auditors to ensure compliance with global standards. They also manage administrative reviews of audit packages and maintain accurate records within internal database systems.
The Senior Digital Marketing Strategist develops and executes digital marketing programs to drive brand awareness, lead generation, and revenue growth. They collaborate with sales and technical teams to create customer-centric digital journeys and optimize marketing performance through data-driven insights.
Design and implement digital and analytical solutions using the Microsoft Power Platform to optimize processes and automate operations. The role focuses on integrating applications and data to drive operational efficiency and business value.
Drive new business opportunities for the Minerals Trade business to achieve revenue targets through client engagement and tailored proposals. Collaborate with internal teams to analyze market trends, generate leads, and transition new accounts to account management.
Prepare and execute product certification processes by interpreting norms and analyzing technical documents. Provide customer support and review test reports and audits to ensure product quality and compliance.
Responsible for receiving, reviewing, and validating startup folders for contractor companies to ensure compliance with established requirements. Provides guidance to contractors on correct documentation and maintains rigorous control records for the accreditation process.
Perform third-party certification audits for food safety and animal feed against standards such as GMP and HACCP. Collect and analyze information to provide certification recommendations and assist in training other auditors.
Perform third-party food safety and animal feed audits against standards like GMP and HACCP to provide certification recommendations. Collaborate with audit teams and assist in training other auditors while maintaining all necessary credentials.
Perform third-party food safety certification audits against standards such as FSSC22000, SQF, and BRC. Collect and analyze information to provide certification recommendations and assist in training other auditors.
Perform professional audits and inspections based on various international standards at client sites. Create detailed audit reports from home to ensure quality, safety, and compliance for clients.
Plan and conduct external quality audits for manufacturing systems in hazardous area environments both in the UK and internationally. Evaluate compliance against industry standards, identify nonconformities, and produce accurate audit reports.
Drive the global standardization and continuous improvement of Knowledge Management and Service Management frameworks. Coordinate operational documentation and manage knowledge repositories to ensure efficiency and compliance across the organization.
Perform audits and certifications for food-related organizations to ensure compliance with quality, safety, and environmental standards. Responsibilities include conducting preliminary research, writing audit reports, and providing direct feedback to clients on findings.
Oversee sterilization processes for medical devices and lead a team of MDR Product Assessors across various certification schemes. Manage resource allocation, drive team performance against global targets, and serve as the senior technical authority for sterilization.
Oversee sterilization processes for medical devices and provide technical support across various certification schemes. Lead a team of Product Assessors and manage resource planning, performance, and regulatory compliance for the sterilization scope.
Oversee sterilization processes for medical devices and lead a team of MDR Product Assessors across various certification schemes. Manage resource allocation, technical guidance, and the development of QMS documentation to ensure regulatory compliance.
Oversee sterilization processes for medical devices and lead a team of MDR Product Assessors across various certification schemes. Act as a senior technical authority and member of the Global Operations Leadership Team to drive performance and regulatory compliance.
Oversee sterilization processes for medical devices and lead a team of Product Assessors across various certification schemes. Act as a senior technical authority and member of the Global Operations Leadership Team to drive performance and regulatory compliance.
Oversee sterilization processes for medical devices and lead a team of Product Assessors across various certification schemes. Manage resource allocation, team performance, and the development of QMS documentation aligned with regulatory requirements.
Oversee sterilization processes for medical devices and lead a team of Product Assessors across various certification schemes. Manage resource allocation, team performance, and the development of QMS documentation aligned with regulatory requirements.
Oversee sterilization processes for medical devices and lead a team of Product Assessors across various certification schemes. Manage resource allocation, team performance, and the development of QMS documentation aligned with regulatory requirements.
Responsible for administering and supervising the Global Quality Management System for mineral geochemistry laboratories in compliance with ISO/IEC 17025. The role involves monitoring laboratory networks, promoting best practices, and leading a virtual team of quality specialists to ensure continuous improvement.
Responsible for administering and monitoring the global Quality Management System for Mineral Geochemistry laboratories in compliance with ISO/IEC 17025. The role involves leading a virtual team of specialists to promote laboratory best practices and a culture of continuous improvement.
Perform safety assessments and certifications for industrial machinery and semiconductor manufacturing equipment based on domestic and international standards. Conduct on-site inspections, risk assessments, and provide external training or seminars on product safety standards.
Drive the global standardization and continuous improvement of Knowledge and Service Management frameworks. Coordinate operational documentation and administer digital knowledge repositories to ensure efficiency and compliance.
Drive the standardization and continuous improvement of Knowledge Management and Service Management frameworks. Partner with stakeholders to ensure operational documentation supports service delivery, compliance, and efficiency.
Drive the standardization and continuous improvement of Knowledge and Service Management frameworks. Partner with stakeholders to ensure operational documentation supports service delivery, compliance, and efficiency.
Perform audits and certifications for food-related companies to ensure compliance with quality, safety, and environmental standards. Responsibilities include conducting preliminary research, writing audit reports, and providing oral feedback on findings.
Drive new business opportunities for the Minerals Trade business to achieve revenue targets through client engagement and tailored proposals. Collaborate with internal teams to analyze market trends, generate leads, and ensure a smooth transition of new accounts to management.
Conduct InfoSec management system audits (ISO/IEC 27001, ISO 22301) for enterprises in Poland and abroad. Prepare post-audit documentation in English and participate in product development and client training.
Conduct InfoSec management system audits (ISO/IEC 27001, ISO 22301) for enterprises in Poland and abroad. Prepare post-audit documentation in English and participate in product development and client training.
Conduct InfoSec management system audits (ISO/IEC 27001, ISO 22301) for enterprises in Poland and abroad. Prepare post-audit documentation in English and participate in product development and client training.
Conduct InfoSec management system audits (ISO/IEC 27001, ISO 22301) for enterprises in Poland and abroad. Prepare post-audit documentation in English and participate in product development and client training.
Conduct InfoSec management system audits (ISO/IEC 27001, ISO 22301) for enterprises in Poland and abroad. Prepare post-audit documentation in English and participate in product development and client training.
Conduct InfoSec management system audits (ISO/IEC 27001, ISO 22301) for enterprises in Poland and abroad. Prepare post-audit documentation in English and participate in product development and client training.
Conduct InfoSec management system audits (ISO/IEC 27001, ISO 22301) for enterprises in Poland and abroad. Prepare post-audit documentation in English and participate in product development and client training.
Conduct certification, labeling, and compliance audits within the automotive sector and manage the technical follow-up of these standards. Responsibilities include analyzing collected data, evaluating client certification eligibility, and contributing to the development of audit schemes.
Responsible for selling environmental analytical services to existing and prospective customers to meet revenue targets. The role involves managing a client portfolio, building long-term relationships, and liaising between customers and lab operations.
Strategically modernize and automate input processes to increase operational efficiency and reduce manual activities. Lead RPA initiatives and integrate workflows between Fiscal, Accounting, Purchasing, IT, and Controlling departments.
Provide administrative support to the inspection team, suppliers, and clients by managing schedules and field activities. Coordinate inspector vacations, handle onboarding for new hires, and report operational issues to management.
The Global Team Leader will manage the IVDR product assessor team and provide technical expertise to the global medical devices network to ensure regulatory compliance. They will also oversee conformity assessment processes, develop training programs, and contribute to the business development of in vitro diagnostic medical device activities.
The Global Team Leader will manage the IVDR product assessor team and provide technical expertise to ensure compliance with in vitro diagnostic medical device regulations. They will also lead business development activities and maintain QMS documentation to meet operational and financial targets.
Lead the global IVDR product assessor team and provide technical expertise for in vitro diagnostic medical device certification processes. Manage regulatory compliance, training programs, and business development activities to meet operational and financial targets.
Lead the global IVDR product assessor team and provide technical expertise for in vitro diagnostic medical device certification processes. Manage regulatory compliance, training programs, and business development activities to meet operational and financial targets.
Lead the global IVDR product assessor team and provide technical expertise for in vitro diagnostic medical device certification processes. Manage regulatory compliance, training, and business development activities to ensure operational and financial targets are met.
Lead the global IVDR product assessor team and provide technical expertise to the medical devices network to ensure regulatory compliance. Manage conformity assessment processes, develop training programs, and contribute to the business development and operational targets of the IVDR division.
The role is responsible for leading the global sales strategy and business development for medical devices, including market analysis and pricing. It involves managing global teams, driving growth, and ensuring alignment with regulatory and commercial objectives.
The role is responsible for leading the global sales strategy and business development for Medical Devices, including market analysis and pricing. It involves managing global teams, driving growth across medical schemes, and ensuring alignment with regulatory and commercial objectives.
The role is responsible for leading the global sales strategy and business development for Medical Devices, including market analysis and pricing. It involves managing global teams, driving growth, and ensuring alignment with regulatory and commercial objectives across all medical schemes.
The role is responsible for leading the global sales strategy and business development for medical devices, including market analysis and pricing. It involves managing global teams, driving growth, and ensuring alignment with regulatory and commercial objectives.
The role is responsible for leading the global sales strategy and business development for medical devices, including market analysis and pricing. It involves managing global teams, driving growth, and ensuring alignment with regulatory and commercial objectives across all medical schemes.
The role is responsible for leading the global sales strategy and business development for Medical Devices, including market analysis and pricing. It involves managing global teams, driving growth across medical schemes, and ensuring alignment with regulatory and commercial objectives.
The role involves leading the global sales strategy for medical devices and driving business development initiatives. It includes market analysis, pricing strategies, and ensuring alignment with business needs to foster growth and enhance client engagement.
The role involves conducting safety assessments for industrial machinery, such as semiconductor manufacturing equipment, based on domestic and international product safety standards, primarily through on-site inspections. Responsibilities also include certification work under schemes like CB and NRTL, and conducting external training and seminars on product safety standards interpretation.
The recruiter will partner with business stakeholders to find hard-to-find candidates for corporate and strategic roles across all business lines, supporting growth plans. This involves acting as a Talent Acquisition Business Partner, managing the end-to-end recruitment process, and developing talent acquisition projects globally.
The main responsibility involves executing design and effectiveness tests for the Internal Controls over Financial Reporting (ICOFR) program according to global requirements and reporting results on time. This includes developing action plans with relevant areas to mitigate risks and supporting internal and external audits.
The main responsibility involves executing design and effectiveness tests for the Internal Controls Over Financial Reporting (ICOFR) program according to global requirements and reporting results on time. This includes developing action plans with relevant areas to mitigate risks and supporting internal and external audits.
The recruiter will partner with business stakeholders to find hard-to-find candidates for corporate and strategic roles across all business lines, supporting growth plans. Responsibilities include acting as a Talent Acquisition Business Partner, managing the end-to-end recruitment process, and developing talent acquisition projects globally.
The role involves conducting safety inspections for industrial machinery, such as semiconductor manufacturing equipment, based on domestic and international product safety standards. Responsibilities also include certification work under schemes like CB and NRTL, and conducting external training and seminars on product safety standards interpretation.
Conduct certification and compliance audits primarily in the automotive sector. Engage with clients to assess their readiness for certification and provide technical follow-up on relevant standards.
