The Social Compliance Auditor will independently plan, conduct, and report on social-compliance and responsible-sourcing audits at various operational facilities. They are responsible for assessing labor practices, human rights, and environmental management while maintaining professional independence and clear communication.
The Lead Auditor is responsible for developing audit scopes, managing audit teams, and assessing management system conformance to aerospace standards. They document audit results, prepare reports, and assist in the training and evaluation of other auditors.
Perform lead audits and assessments for ISO 14001, 45001, and RC standards to ensure customer compliance and quality. Evaluate customer needs and satisfaction while maintaining a professional image in a virtual and travel-based environment.
Perform independent management system assessments and ISO 9001:2015 audits at client locations. Collaborate with schedulers to ensure audits are conducted as specified to help clients improve business processes.
Perform medical device audits at client locations and manage audit team activities. Develop audit scopes and plans while presenting conclusions and reviewing nonconformity resolutions with customers.
Conduct aerospace management system audits and manage audit team activities to ensure compliance. Develop audit scopes and plans while presenting conclusions and reviewing nonconformity resolutions with customers.
Drive revenue growth by identifying and closing new business opportunities for sustainability assurance, verification, and audit services across the US. Develop and execute a sales strategy targeting various industries while managing the pipeline through HubSpot.
Responsible for reviewing technical documentation and conducting audits for medical devices under MDR, ISO 13485, and MDSAP. The role involves assessing product changes, managing audit programs, and collaborating with experts to ensure regulatory compliance and final product approval.
The role involves reviewing technical documentation and conducting audits for medical devices according to MDR and ISO 13485 standards. Responsibilities include assessing product changes, managing audit programs, and collaborating with experts to ensure regulatory compliance and final product approval.
