Cork, Ireland
Internship Explorer
Internship Explorer
The Quality and Regulatory Intern will support McKesson Global Sourcing Limited [Irish Branch] in maintaining high-quality standards and ensuring compliance with relevant regulatory requirements for medical devices and pharmaceutical products. This role offers hands-on experience in a dynamic global sourcing environment. Assist in the review and maintenance of quality management system (QMS) documentation, including procedures, work instructions, and records. Support regulatory affairs activities, such as preparing documentation for product registrations, renewals, and amendments. Conduct research on global regulatory requirements and industry standards applicable to medical devices and pharmaceuticals. Participate in internal audits and support external audit preparations, ensuring compliance with ISO 13485, MDR, IVDR, and other relevant regulations. Assist in the investigation of quality issues, non-conformances, and customer complaints, including root cause analysis and corrective/preventive actions (CAPA). Collaborate with cross-functional teams, including Sourcing, Supply Chain, and Legal, to ensure quality and regulatory compliance throughout the product lifecycle. Maintain accurate and up-to-date databases for regulatory submissions, product registrations, and quality records. Support the creation and review of technical documentation, such as product specifications and labeling. Perform administrative tasks as needed to support the Quality and Regulatory team.
