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Regulatory Affairs Specialist

2 mesi fa

Pomezia, Lazio, Italia STERIS A tempo pieno
{"Job Summary

We are seeking a highly motivated and detail-oriented Regulatory Affairs Intern to join our team at STERIS. As a Regulatory Affairs Intern, you will play a critical role in supporting the implementation of efficient and effective processes to obtain and maintain clearance to market STERIS products globally.

Key Responsibilities

* Develop a working knowledge of regulatory requirements and standards associated with the European Union, including the Medical Device Directive 93/42/EC and the EU MDR Regulation 2017/745
* Assist in the preparation, monitoring, and maintenance of documents for submissions to regulatory agencies
* Support the duties of the functional areas, including registration and technical duties
* Maintain understanding of and compliance with all current active Corporate Procedures
* Protect company confidential information

Requirements

* High School Diploma or GED
* Bachelor's Degree in Engineering General or Biology
* Excellent PC skills, including Microsoft Office applications
* Italian mother tongue and English fluent

Competencies

* Strong interpersonal skills
* Self-starter that is highly organized
* Strong oral and written communication skills

About STERIS

STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. We are committed to equal employment opportunity and the use of affirmative action programs to ensure that persons are recruited, hired, trained, transferred, and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, sex, sexual orientation, gender identity, genetic information, and any other category protected by state or local law.

Equal Opportunity Employer

STERIS is an Equal Opportunity Employer.