Regulatory Affairs Intern
Pubblicato il 16-08-2026 - Steris in Roma
At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe.
Position Summary
We are looking for a candidate that will join our team as Regulatory Affairs Intern (stage).
The mission of the STERIS Regulatory Affairs function is to implement efficient and effective processes to initially obtain and then maintain clearance to market STERIS products in support of STERIS’s global business plans. This includes determining submission to NB for the CE marking and in some cases of registration and/or submission requirements in the International markets, working with STERIS International Registration staff to identify requirements in other targeted markets, and working with product acquisition or development teams to ensure these requirements are met. This group also identifies and supports Regulatory Compliance needs.
The Regulatory Affairs Intern will develop a working knowledge of the following market and the regulations and standards associated:
- Europe/Middle East/Africa (EMEA)
- European Union: Medical Device Directive 93/42/EC as amended by 2007/47/EC and EU MDR Regulation 2017/745
Key International Standards:
- ISO 13485: Medical devices – Quality management systems;
- ISO 9001: Quality management systems;
- ISO 14971 Application of Risk Management to Medical Devices.
The Regulatory Affairs Intern will have responsibility to support the duties of the functional areas described below, as assigned, under the guidance and direction of his/her manager and other senior Regulatory Affairs staff.
General Duties
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Support compliance with corporate procedures and company policies.
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Handle confidential information appropriately under supervision.
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Assist with daily tasks and assigned projects.
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Contribute to maintaining a safe and compliant work environment.
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Support updates of GSPR checklists and EU technical documentation.
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Assist with regulatory chan