Director of Regulatory Affairs Jobs in Minnesota
Piper Companies is currently looking for an experienced Associate Director of Regulatory Affairs in Eden Prairie, Minnesota (MN) to work for an innovative and growing pharmaceutical manufacturer....
Strong working knowledge of FDA regulations, guidance documents, and pre-submission processes. Experience supporting design controls, risk management, and quality system activities....
Job Title: Director of Regulatory Affairs Job Description We are seeking an experienced Director of Regulatory Affairs to create and execute global regulatory strategies for our products, in alignment...
Director of Regulatory Affairs Structural Heart | Medical Device | Relocation Offered Job Description We are seeking an experienced Director of Regulatory Affairs to create and execute global regulatory...
Strong knowledge of global regulatory standards and quality systems, including ISO 13485, GMP, GCP, GLP, QSR, and MDR....
Strong working knowledge of FDA regulations, guidance documents, and pre-submission processes. Experience supporting design controls, risk management, and quality system activities....
Job Title:Associate Director, Regulatory Affairs Work Type:Work Days: Work Vary: No, Shift: First (Day), Hours Per Week: 40, Work Type: Regular Salary Offered:Unspecified Benefits:Unspecified....
Keywords: Regulatory Affairs, Biologics, Pharmaceuticals, IND Submission, eCTD Format, ESG Portal, FDA Regulations, Clinical Development, Organ Transplant, Bioengineered Organs, Tissue Engineering,...
Demographic Data for Minnesota
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Salary for Director of Regulatory Affairs Jobs in Minnesota
Required or preferred licenses and certifications for Director of Regulatory Affairs positions.
Highest Education Level
Director of Regulatory Affairss in Minnesota 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
- Oncology
- Medical Device Sales
- Document Management
- Clinical Trials
- Product Launch
- Good Manufacturing Practices
- Clinical Research
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- 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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