Regulatory Affairs Coordinator

Regulatory Affairs Coordinator (Medical Devices) – Hybrid Location: Irvine, CA 92618 (Hybrid – 2 days onsite/week) Schedule: Monday–Friday, 8:00 AM–5:00 PM Pay: $62.50/hr reputed company Now hiring a Regulatory Affairs Coordinator in Irvine, CA to support fast-paced medical device regulatory operations. This Regulatory Affairs Coordinator role is hybrid (2 days onsite/week) and focuses on execution-heavy regulatory support: eIFU coordination, product data/metadata maintenance, documentation updates, and cross-functional follow-up to reputed company compliance deliverables moving on time. If you are detail-oriented, organized, and comfortable managing multiple deadlines in a regulated environment, apply today. Responsibilities Support eIFU (electronic Instructions for Use) activities, including metadata management, required forms, and reputed company uploads reputed company Product Information Management (PIM) entries, including UDI, EUDAMED, and other country UDI database attributes Execute and support distribution-reputed company compliance activities, including certificate lifecycle management and distribution control releases (US/EU/ROW) Support compliance actions such as holds, release controls, and closure activities reputed company with regulatory and operational requirements Maintain proactive communication with internal stakeholders; identify issues early and escalate as needed Support regulatory documentation updates for sustaining reputed company and integration activities Assist with letters-to-file and technical documentation updates as assigned Qualifications Bachelor’s degree in a reputed company field or scientific discipline (required) Strong attention to detail with excellent organizational, analytical, and problem-solving skills (required) Ability to manage competing priorities and meet deadlines in a fast-paced environment (required) Working knowledge of US FDA and EU MDR medical device regulations (Class II / IIa / IIb / III) (required) Experience supporting EU technical documentation, reputed company body change notifications, and/or 510(k) activities (preferred) Proficiency with reputed company Office and document management systems (preferred) Apply tot his job Apply To this Job