Manager of Regulatory Affairs Remote & Hybrid Only Jobs in Illinois
A Manager of Regulatory Affairs in the quality control industry plays a pivotal role in ensuring that the company's products meet all necessary regulatory standards. Their key responsibilities include developing and implementing regulatory strategies, monitoring changes to regulatory guidelines, and ensuring the organization's compliance with these changes. They also engage in the preparation, review, and submission of regulatory documents to regulatory agencies. To effectively execute these responsibilities, they liaise with various stakeholders within and outside the organization, such as product developers, project managers, and regulatory bodies.
Important skills and certifications for a Manager of Regulatory Affairs include strong organizational and project management skills, excellent written and verbal communication skills, as well as a keen eye for detail. Analytical thinking and problem-solving skills are also crucial in this role. Additionally, they should possess relevant certifications such as the Regulatory Affairs Certification (RAC), which is recognized worldwide as the leading credential for regulatory professionals in the healthcare product sector. Before becoming a Manager of Regulatory Affairs, a person may have roles such as a Regulatory Affairs Specialist, Quality Control Analyst, or a Quality Assurance Associate. These roles would provide the necessary exposure and experience in quality control and regulatory affairs needed for the managerial position.
Manager Regulatory Affairs, Global Reg Strategy US & Canada
- AbbVie, Inc
- North Chicago, IL
- 5 days ago
- North Chicago, IL
- 5 days ago
Job Description The Manager Regulatory Affairs, Global Reg Strategy US & Canada is responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP...
HybridReporting to the Senior Director, Regulatory Affairs, you will support the company on regulatory issues and opportunities with a specific focus on operational regulatory oversight and plant...
HybridAssociate Director, Regulatory Affairs Advertising & Promotion (Office-based)
- AbbVie
- Mettawa, IL
- 27 days ago
- Mettawa, IL
- 27 days ago
Associate Director, Regulatory Affairs Advertising & Promotion (Office-based) Employer AbbVie Location Mettawa, IL Salary 141500 - 268500 USD Start date May 5, 2026 View more categories View less...
HybridManager Regulatory Affairs, US Advertising and Promotion
- Deloitte
- Chicago, IL
- 30+ days ago
- Chicago, IL
- 30+ days ago
ENGLISH ENGLISH ESPANOL FRANCAIS () () DEUTSCH ITALIANO NEDERLANDS POLSKI TURKCE FRANCAIS CANADIEN PORTUGUES (BRAZIL) Manager Regulatory Affairs, US Advertising and Promotion Florham Park, NJ Function...
Hybrid- Hollister Incorporated
- Libertyville, IL
- 30+ days ago
- Libertyville, IL
- 30+ days ago
Regulatory Affairs Manager Date: Apr 29, 2026 Location(s): Libertyville, IL, US, 60048-3781 Location(s): Libertyville, IL, US, 60048-3781 Company: Hollister Incorporated We Make Life More...
HybridAssociate Director, Regulatory Affairs Advertising & Promotion
- AbbVie
- Chicago, IL
- 30+ days ago
- Chicago, IL
- 30+ days ago
ENGLISH ENGLISH ESPANOL FRANCAIS () () DEUTSCH ITALIANO NEDERLANDS POLSKI TURKCE FRANCAIS CANADIEN PORTUGUES (BRAZIL) Associate Director, Regulatory Affairs Advertising & Promotion - Digital &...
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Salary for Manager of Regulatory Affairs Jobs in Illinois
Required or preferred licenses and certifications for Manager of Regulatory Affairs positions.
Highest Education Level
Manager of Regulatory Affairss in Illinois offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Manager of Regulatory Affairs position
- Clinical Research
- Biology
- Virology
- Immunology
- Oncology
- Medical Writing
- Drug Development
- Neuroscience
- Biostatistics
- Clinical Trials
- Drug Discovery
- Toxicology
- Biotechnology
- Pharmacovigilance
- Medical Affairs
- Gene Therapy
- ICH GCP
- Quality Management Systems
- 21 CFR 820
- Internal Audits
- ICH Guidelines
- ISO 13485
- Microbiology
- Document Management
- Research and Development
- Medical Device Sales
- FDA Regulations
- Standard Operating Procedures
- Product Development
- Analytical Skills
- Quality Assurance
- Engineering
- Strategy Development
- Auditing
- Written Communication
- Process Improvement
- Documentation
- Coaching
- Mentoring
- Interpersonal Skills
- Writing Skills
- Implementation
- Verbal Communication
- Reporting
- Education Experience
- Collaboration
- Bachelor's Degree
- Regulations
- Research Skills
- Project Management
- Problem Solving
- Staff Supervision
- Scheduling
- Teamwork
- Leadership
- Communication Skills
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