Manager of Regulatory Affairs Jobs in Delaware
Regulatory Affairs Manager, Designed Enzymatic Biomaterials
- Wilmington, DE
- 12 days ago
- Wilmington, DE
- 12 days ago
In the Global Regulatory Affairs (GRA) team, we have an opening for a Manager, Regulatory Affairs to drive project management, regulatory, technical and other activities for our Designed Enzymatic Biomaterials...
The Associate Manager, Regulatory Affairs will combine expertise in knowledge management and regulatory documentation with strong project management skills to build a robust infrastructure that supports...
As we create a colorful, capable and cleaner world through chemistry, we invite you to join our team to harness the power of chemistry to shape markets, redefine industries and improve lives for...
Regulatory Affairs Manager (m/w/d) BIOTRONIK ist einer der weltweit fuhrenden Hersteller kardio- und endovaskularer Implantate und Katheter fur Herzrhythmusmanagement, Elektrophysiologie und...
regulations, including 21 CFR 1271 and 21 CFR 312 **Job Location** This role is located onsite in our Eden Prairie, MN (Miromatrix) location with the option for a remote candidate with monthly travel...
Regulatory Affairs Manager Location: Hybrid remote with 2-3 per week in office, must reside in a service area state commutable to Dover, DE; West Palm, FL; or Yulee, FL office locations What makes...
In-depth knowledge of global regulatory frameworks, including ICH, GCP, EU Clinical Trial Regulation (CTR), and US FDA regulations....
HR Control Manager - Regulatory Affairs - Vice President
- Newark, DE
- 45+ days ago
- Newark, DE
- 45+ days ago
JobID: 210574564 Category: Control Officers JobSchedule: Full time Posted Date: 2025-06-18T04:00:00+00:00 JobShift: Day Base Pay/Salary: Jersey City,NJ $118,750.00-$190,000.00 Join our HR Control...
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Manager of Regulatory Affairss in Delaware offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Manager of Regulatory Affairs position
- Gene Therapy
- Supplier Auditing
- Medical Affairs
- Drug Discovery
- 21 CFR 820
- Internal Audits
- Pharmacovigilance
- ICH Guidelines
- Drug Development
- Immunology
- Change Control
- GxP
- Quality Systems
- Biochemistry
- ISO 13485
- Biotechnology
- Quality Management Systems
- Biology
- Product Launch
- Medical Device Sales
- Document Management
- Clinical Trials
- Research and Development
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- FDA Regulations
- Standard Operating Procedures
- Product Development
- Masters In Education
- Engineering
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- Implementation
- Written Communication
- Military Background
- Auditing
- Verbal Communication
- Education Experience
- Collaboration
- Documentation
- Mentoring
- Interpersonal Skills
- Reporting
- Employee Development
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- Coaching
- Filing
- Policy Development
- Problem Solving
- Bachelor's Degree
- Regulations
- Project Management
- Microsoft Excel
- Time Management
- Research Skills
- Teamwork
- Staff Supervision
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- Leadership
- Communication Skills
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