Regulatory Affairs Specialist Jobs in Kansas
The Director of Regulatory Affairs in the quality control industry plays an essential role in ensuring that the company's products meet all regulatory standards and compliance requirements. This individual oversees the development and implementation of regulatory strategies for new and existing products, supervises the preparation of regulatory submissions, and maintains communication with regulatory authorities. They also monitor changes in regulations, interpret these updates for relevant departments within the company, and implement necessary changes to maintain compliance. They are responsible for setting the company's standards for quality, safety, and efficacy.
To excel in this role, one should possess excellent analytical skills, strategic thinking, and strong leadership abilities. A deep understanding of regulatory guidelines, ability to interpret complex regulations, and excellent communication skills are essential. They should have a degree in a relevant field, along with certifications such as Regulatory Affairs Certification (RAC), Certified Quality Auditor (CQA), and Certified Quality Engineer (CQE). Prior to becoming a Director of Regulatory Affairs, individuals might have roles such as Regulatory Affairs Specialist, Regulatory Affairs Manager, or Quality Control Manager.
Required Skills & Education Bachelor's degree (or relevant financial services experience) Experience with internal audit methodology and applying concepts in audit delivery and execution Solid understanding...
Carrington Remote IT Quality Assurance and Compliance, Analyst in Topeka , Kansas Come join our amazing team and work remote from home! What you'll do: Responsible for the timely and accurate...
Remote WorkA specialist in the field of Compliance/Audit. Knows how to apply theory and put it into practice with an in-depth understanding of a specific area. Independently performs the full range of...
Job Description GRA Operations GRA Operations is part of Global Regulatory Affairs Biologics & Operations Animal Health. This department is responsible for the global regulatory IT landscape and...
Compliance Analyst Sr--Medical Pharmacy Specialty/Medicare Part B- REMOTE
- Topeka, KS
- 11 days ago
- Topeka, KS
- 11 days ago
Our work matters. We help people get the medicine they need to feel better and live well. We do not lose sight of that. It fuels our passion and drives every decision we make. Job Posting Title...
Remote Workaudits and assessments to identify areas of improvement and implement corrective actions Provide guidance and facilitate to internal stakeholders on trade compliance matters, including training and...
Invite a friend Job Description DEMDACO is a gift and home decor company based in Leawood, KS. We strive to 'lift the spirit' with our customers, consumers and colleagues. ' Products are curated...
Information Security & Compliance Analyst (12 mo. contract)
- Kansas City, KS
- 45+ days ago
- Kansas City, KS
- 45+ days ago
Management and Environmental Management....
Sr. Compliance Analyst USA Remote 1 item added ID: 8491 Job Description Symetra has an exciting opportunity to join our Corporate Compliance team as a Senior Compliance Analyst! About the role As...
When applicable, Bombardier promotes flexible and hybrid work policies. Why join us? Bombardier is a global leader in aviation, focused on designing, manufacturing and servicing the world's most...
Demographic Data for Kansas
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Regulatory Affairs Specialist Online Courses and Training Opportunities
Salary for Regulatory Affairs Specialist Jobs in Kansas
Required or preferred licenses and certifications for Regulatory Affairs Specialist positions.
Highest Education Level
Regulatory Affairs Specialists in Kansas offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Regulatory Affairs Specialist position
- Analytical Skills
- Filing
- Financial Services
- Mortgage Processing
- Reimbursement
- Juris Doctor
- Internal Audits
- Quality Systems
- 21 CFR 820
- ISO 9001
- ICH Guidelines
- ISO 13485
- ISO 14001
- Quality Management
- Process Controls
- Medical Device Sales
- Business Processes
- FDA Regulations
- Microsoft Visio
- Standard Operating Procedures
- Engineering
- Product Development
- Affirmative Action
- Risk Management
- Quality Assurance
- Process Improvement
- Implementation
- Military Background
- Auditing
- Investigation
- Written Communication
- Verbal Communication
- Documentation
- Collaboration
- Interpersonal Skills
- Reporting
- Education Experience
- Bachelor's Degree
- Regulations
- Microsoft PowerPoint
- Policy Development
- Project Management
- Microsoft Office
- Microsoft Excel
- Problem Solving
- Time Management
- Teamwork
- Research Skills
- Staff Supervision
- Organization
- Scheduling
- Leadership
- Communication Skills
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