- Cleveland Clinic (Mayfield Heights, OH)
- …assure quality care. Facilitates appropriate length of stay, discharge planning and compliance with regulatory standards for inpatient management. May serve as ... clinical preceptor for PA/APRN students and other health professionals. May serve as Faculty for onboarding new employees. Demonstrates a high standard of moral and ethical behavior. Demonstrates compassion and professionalism and a commitment to excellent… more
- Cleveland Clinic (Mayfield Heights, OH)
- …assure quality care. + Facilitates appropriate length of stay, discharge planning and compliance with regulatory standards for inpatient management. May serve as ... clinical preceptor for PA/APRN students and other health professionals. + May serve as Faculty for onboarding new employees. + Demonstrates a high standard of moral and ethical behavior. + Demonstrates compassion and professionalism and a commitment to… more
- Medtronic (Santa Rosa, CA)
- …solutions. This role will be based in Santa Rosa, CA. The **Principal Regulatory Affairs Specialist ** will support Research and Development programs with early ... global regulation and guidance updates in the digital health space. Additionally, the Principal Regulatory Affairs Specialist is expected to play a key role in… more
- Teleflex (Morrisville, NC)
- Regulatory Affairs Specialist **Date:** Sep 9, 2025 **Location:** Morrisville, NC, US **Company:** Teleflex **Expected Travel** : Up to 10% **Requisition ID** ... solutions that make a difference in patients' lives. **Position Summary** The Regulatory Affairs Specialist will develop strategies and submissions for projects… more
- Abbott (St. Paul, MN)
- …female executives, and scientists **The Opportunity** We are seeking a **Principal Regulatory Affairs Specialist ** to join Abbott's Vascular Division on-site in ... vascular disease. As an experienced individual contributor, a Principal Regulatory Affairs Specialist is to provide support...+ Minimum of 5 years' experience working with Class II and/or Class III medical devices. Regulatory … more
- Abbott (Alameda, CA)
- …with outside regulatory agencies and trade associations, develop innovative regulatory compliance strategy, and provide executive management with ... regulatory submission. . Write and edit technical documents. . Administer/meet regulatory requirements to achieve excellent compliance status with no… more
- Abbott (Alameda, CA)
- …regulatory submission. + Write and edit technical documents. + Administer/meet regulatory requirements to achieve excellent compliance status with no ... (98/79/EC). **Preferred** **Qualifications** + 5 years' experience working with Class II , Class III medical devices and/or biologics/drugs. Regulatory Affairs… more
- Globus Medical, Inc. (Audubon, PA)
- …needed for IDE and PMA reporting + Reviews Document Change Orders for Regulatory compliance , including drawings and labeling changes + Performs routine ... their lives as quickly as possible. **Position Summary:** The Regulatory Affairs Specialist assists with drafting, submitting...to the Food and Drug Administration (FDA) for class II and class III products. This position entails development… more
- Stryker (Redmond, WA)
- We are currently seeking a **Senior Regulatory Affairs Specialist ** to join our **Medical** **Division** to be based **Hybrid** Monday through Wednesday in ... + Evaluate product classification and jurisdiction, and determine appropriate regulatory pathways and compliance requirements (local, national, international)… more
- Abbott (Plymouth, MN)
- …with their lives. **The Opportunity** Abbott is seeking a passionate, experienced **Senior Regulatory Affairs Specialist ** to join our team on-site in Plymouth, ... MN. In this role, you will lead the preparation and submission for regulatory approvals and identify and resolve problems. You will provide regulatory guidance… more
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