Teams at Medtronic

Support regional statutory accounting, month-end close, financial reporting and reconciliations. Coordinate statutory and tax audits, ensure IFRS compliance (including IFRS 15), investigate variances, maintain controls, and partner with stakeholders to improve reporting and processes.

Supports regulatory affairs for medical device and pharmaceutical projects, including global registration submissions, marketing authorizations, regulatory strategy, health authority communications, clinical and preclinical document review, change-control assessments, labeling and promotional material compliance, regulatory inspections, audits, and maintenance of regulatory records. Requires international regulatory knowledge, strong communication and organizational skills, and the ability to manage multiple priorities in a cross-functional environment.

Support clinical data collection and management for studies: design and implement protocols and CRFs, test and validate reports/dashboards (SQL, Spotfire, Power BI), develop data quality plans, review and resolve discrepancies, and prepare internal validation reports. Entry-level individual contributor role with mentorship and close supervision.