Regulatory Affairs Specialist

Description

The Regulatory Affairs position within Regulatory Policy & Intelligence (RP&I) is responsible for contributing to or leading impact assessments and for changes to regulatory requirements, assessing applicability regarding regulatory submissions and procedures, and assessing the timeline for implementation of changes. This role may also help monitor for changes to regulatory requirements and working with other Subject Matter Experts to ensure requirements are appropriately translated into the quality management system. This position may require support from senior Regulatory Affairs members and / or managers.

This role can also be based in St. Louis.

Job Duties

• Organize, update, and maintain regulatory documentation in accordance with company policy and procedures.
• Perform and / or assist in the completion of the following tasks :
• Monitoring of changes to existing regulatory requirements or identifying new regulatory requirements.
• Assessment of impact of new or revised regulatory requirements.
• Collaboration with SME's to provide feedback and / or create supporting documentation to ensure product deliverables meet Health Authority expectations.
• Coordination with global / local RA counterparts to ensure that changes to regulatory requirements are understood.
• Conduct research about new regulations and guidance documents.
• Development and review of corporate and department procedures.
• Assist or participate in audits when needed.
• Support or lead in understanding regulatory requirements and identify solutions; provide possible suggestions for implementation.
• Ensures accurate tracking of new or revised regulatory requirements.
• Lead and / or coordinate meetings and guide discussions regarding regulatory topics.

Qualifications :

Bachelor's Degree required. Science background is preferred.

Specialist :

3+ years in regulatory affairs, medical device / IVD industry required.

3+ years in FDA environment preferred.

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BioMerieux Inc. and its affiliates are Equal Opportunity / Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant's identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMerieux's or its affiliates' application process by contacting us via telephone at , by email at [emailprotected], or by dialing 711 for access to Telecommunications Relay Services (TRS).