Regulatory Affairs Specialist Jobs in Gladstone, MO
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.
Regulatory Affairs Coordinator - Clinical Laboratory
- Kansas City, KS (7 miles from Gladstone, MO)
- 17 hours ago
- Kansas City, KS (7 miles from Gladstone, MO)
- 17 hours ago
Acts as a superuser of the laboratory quality management software. Manage delegation of duties and other required personnel documentation....
- Kansas City, MO (7 miles from Gladstone, MO)
- 2 days ago
- Kansas City, MO (7 miles from Gladstone, MO)
- 2 days ago
, a division of UMB Bank n.a. Are you ready to be part of something more? You're more than a means to an end-a way to help us meet the bottom line. UMB isn't comprised of workers, but of people...
International Trade Compliance Analyst 2
- Lenexa, KS (21 miles from Gladstone, MO)
- 28 days ago
- Lenexa, KS (21 miles from Gladstone, MO)
- 28 days ago
Overview We are seeking a full-time International Trade Compliance Analyst 2 in our Olathe, KS location. In this role, you will be responsible for working globally with multiple departments/teams...
- Kansas City, MO (7 miles from Gladstone, MO)
- 28 days ago
- Kansas City, MO (7 miles from Gladstone, MO)
- 28 days ago
Corporate Compliance Services partners with UMB management in its obligation to effectively manage compliance and related risks within the UMB family of corporations. This team provides timely,...
NERC Compliance Analyst - Substation
- Kansas City, MO (7 miles from Gladstone, MO)
- 45+ days ago
- Kansas City, MO (7 miles from Gladstone, MO)
- 45+ days ago
REQUISITION: TRA00XJ DEPARTMENT: Substation C&M Technical Support - Topeka Operations Center, Manhattan Service Center, Wichita Service Center, 930 N Olive LOCATION: Topeka, KS Manhattan, KS...
- Kansas City, MO (7 miles from Gladstone, MO)
- 60+ days ago
- Kansas City, MO (7 miles from Gladstone, MO)
- 60+ days ago
Canadian Pacific (CP) and Kansas City Southern (KCS) are now CPKC. As the only truly North American railway, we are making big moves! Drawing on our strong foundations and heritage, CPKC moves...
Demographic Data for Gladstone, MO
Moving to Gladstone, MO? Find some basic demographic data about Gladstone, MO below.
Regulatory Affairs Specialist Online Courses and Training Opportunities
Salary for Regulatory Affairs Specialist Jobs in Gladstone, MO
Required or preferred licenses and certifications for Regulatory Affairs Specialist positions.
Highest Education Level
Regulatory Affairs Specialists in Gladstone, MO offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Regulatory Affairs Specialist position
- Finance
- Internal Control
- Reimbursement
- Institutional Review Board
- Internal Audits
- 21 CFR 820
- ICH Guidelines
- Corrective Actions & Preventive Actions
- ISO 13485
- Validation
- Medical Device Sales
- Business Processes
- FDA Regulations
- Document Management
- Microsoft Visio
- Resolution
- Product Development
- Engineering
- Affirmative Action
- Risk Management
- Strategy Development
- Process Improvement
- Military Background
- Implementation
- Analytical Skills
- Auditing
- Investigation
- Written Communication
- Verbal Communication
- Documentation
- Collaboration
- Data Analysis
- Interpersonal Skills
- Reporting
- Education Experience
- Bachelor's Degree
- Filing
- Regulations
- Microsoft PowerPoint
- Policy Development
- Project Management
- Problem Solving
- Microsoft Office
- Microsoft Excel
- Time Management
- Research Skills
- Staff Supervision
- Organization
- Scheduling
- Leadership
- Communication Skills
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