Director of Regulatory Affairs Remote & Hybrid Only Jobs in Illinois
Senior Manager Regulatory Affairs US Advertising and Promotion - Immunology Dermatology (Remote)
- Mettawa, IL
- 6 days ago
- Mettawa, IL
- 6 days ago
Company DescriptionAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive...
Remote WorkAssociate Director, Regulatory Affairs Advertising & Promotion (Hybrid Or Remote)
- Mettawa, IL
- 19 days ago
- Mettawa, IL
- 19 days ago
ASSOCIATE DIRECTOR, REGULATORY AFFAIRS ADVERTISING & PROMOTION (HYBRID OR REMOTE) AbbVie - 3.8 Mettawa, IL Job Details Full-time Estimated: $184K - $220K a year 20 hours ago Benefits Paid holidays Health...
Remote WorkSenior Manager, Regulatory Affairs - Device (Hybrid Onsite)
- North Chicago, IL
- 21 days ago
- North Chicago, IL
- 21 days ago
Understanding of device/combination product regulations [21 CFR Parts 3, 4, GCP, GLP, 210/211, 820 QSR (Design Control), European Medical Device Directives and Regulation (MDR/IVDR), ISO 13485, MDSAP...
at GE HealthCare in Chicago, Illinois, United States Job Description Job Description Summary We are seeking a highly motivated and detail-oriented Regulatory Affairs - CMC professional with a...
Remote WorkWork Location: Chicago Due to the highly interactive and team-based nature of this role, in-person attendance for most of the workweek (i.e., 3 days or more) is essential for: effective...
Senior Manager Regulatory Affairs, CMC and Regulatory Sciences
- Chicago, IL
- 45+ days ago
- Chicago, IL
- 45+ days ago
Description Senior Manager Regulatory Affairs - CMC CMC, and Regulatory Sciences About Us: Founded in 2017 and based in Chicago, Meitheal is focused on the development and commercialization of...
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Director of Regulatory Affairss in Illinois offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Director of Regulatory Affairs position
- Gene Therapy
- Medical Affairs
- ICH Guidelines
- 21 CFR 820
- Pharmacovigilance
- Quality Systems
- ISO 13485
- Medical Writing
- Drug Development
- GxP
- Immunology
- Change Control
- Toxicology
- Biotechnology
- Quality Management Systems
- Biology
- Microbiology
- Oncology
- Medical Device Sales
- Document Management
- Clinical Trials
- Product Launch
- Good Manufacturing Practices
- Clinical Research
- Research and Development
- FDA Regulations
- Resolution
- Standard Operating Procedures
- Product Development
- Strategy Development
- Engineering
- Implementation
- Written Communication
- Military Background
- Analytical Skills
- Auditing
- Verbal Communication
- Collaboration
- Documentation
- Coaching
- Reporting
- Mentoring
- Interpersonal Skills
- Education Experience
- Quality Assurance
- Policy Development
- Filing
- Problem Solving
- Bachelor's Degree
- Project Management
- Regulations
- Microsoft Office
- Research Skills
- Staff Supervision
- Organization
- Teamwork
- Scheduling
- Leadership
- Communication Skills
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