Regulatory Affairs Jobs in Jacksonville
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Search Results - Regulatory Affairs Jobs in Jacksonville
Insmed-Jacksonville
correspondence and submissions accurately; ensure lifecycle management activities
Key requirements
• Bachelor’s degree in a scientific discipline
• 10+ years in Global CMC Regulatory Affairs or relevant pharma/biotech development experience
• 5+ years of gene...
Jacksonville
compliance, legal, risk, audit, regulatory affairs, policy administration, operations, project coordination, governance, or related corporate function.
• Experience supporting obligation tracking, regulatory change monitoring, policy management, disclosure...
crowley.com -
Insmed-Jacksonville
correspondence and submissions accurately; ensure lifecycle management activities
Key requirements
• Bachelor’s degree in a scientific discipline
• 10+ years in Global CMC Regulatory Affairs or relevant pharma/biotech development experience
• 5+ years of gene...
Planet Pharma-Jacksonville
Overview
As Regulatory Submissions Specialist, you will lead the preparation and coordination of document packages for regulatory submissions, including 510(k) and EU MDR strategies. You will work across functions to ensure compliance and timely...
Medline-Jacksonville
Overview
In this remote leadership role you drive global regulatory strategies to bring new medical device products to market and support existing products. You will negotiate with regulators, guide cross-functional teams, and inform product...
Medtronic-Jacksonville
Medical safety and risk management
• Post-market surveillance
• Regulatory affairs knowledge (FDA, EU MDR)...
Illumina-Jacksonville
Management, Regulatory Affairs, Market Access, Legal, Compliance and Commercial teams
• Contribute to publication planning and external scientific communications
• Maintain independence and compliance with regulations governing medical affairs...
Illumina-Jacksonville
Management, Regulatory Affairs, Market Access, Legal, Compliance and Commercial teams
• Contribute to publication planning and external scientific communications
• Maintain independence and compliance with regulations governing medical affairs...
Medtronic-Jacksonville
and lifecycle decision-making
• Respond to safety inquiries from internal stakeholders, healthcare professionals, and regulatory agencies
• Collaborate with Medical Safety, Clinical, Regulatory Affairs, Risk Management, and Quality teams on emerging safety...
Danaher Corporation-Jacksonville
8+ years of progressive experience in quality, audits, regulatory affairs, or related areas within diagnostics, biopharma, medical devices, CROs, or similar regulated industries
• Working knowledge of regulated quality systems and audit practices...
Merck Sharp & Dohme (MSD)-Jacksonville
finance, regulatory affairs, pharmacovigilance, and HQ
• Support team knowledge sharing and buddying within the country operations
Key requirements
• Bachelor's Degree or higher
• 3+ years of experience in negotiating contracts or budgets
• Juris Doctor...
US Pharmacopeia-Jacksonville
advisor to pharmaceutical developers and manufacturers
• Create User Forums, Quality Hours, Workshops and Webinars with Scientific Affairs, Regulatory Affairs to showcase USP value
• Partner with regional distributors for aligned, resource-shared, joint...
Acrisure-Jacksonville
to Regulatory Affairs, Risk, Compliance, Sourcing, HR, etc., with capabilities like template filling, data extraction, contract analysis, drafting, and jurisdictional alignment
• Facilitate ideation sessions and lead technical build-out after teams are trained...
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