Regulatory Affairs Specialist
5 giorni fa
Responsibilities:
* Maintain a deep understanding of EU regulations, including the Medical Device Directive 93/42/EEC and the EU MDR Regulation 2017/745
* Develop and implement effective regulatory strategies to ensure compliance with EU regulations
* Collaborate with cross-functional teams to ensure regulatory requirements are met
* Prepare and submit regulatory documents, including CE marking and registration submissions
* Monitor and maintain up-to-date knowledge of regional and national regulations
Requirements:
* Bachelor's degree in Biological Science or related field
* Excellent PC skills, including Microsoft Office applications
* Italian mother tongue and English fluent
* International regulatory experience
* Ability to work closely with people at all levels within the Steris organization
If you are a motivated and detail-oriented individual with a passion for regulatory affairs, we encourage you to apply for this exciting opportunity.
At Steris Canada Corporation, 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.
We are a leading global provider of products and services that support patient care with an emphasis on infection prevention.
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