Quality Systems Engineer Jobs in Apopka, FL
A Regulatory Affairs Specialist in the quality control industry is responsible for ensuring that an organization's products comply with all applicable domestic and international regulatory standards and guidelines. They play a crucial role in the product development process by providing regulatory guidance and strategies, preparing and submitting documentation for regulatory approvals, liaising with regulatory authorities, and maintaining knowledge of evolving regulatory requirements. They may also be involved in reviewing marketing materials, training materials, and product labels to ensure regulatory compliance.
A Regulatory Affairs Specialist should possess strong analytical, communication, and project management skills. They must be detail-oriented, with a strong understanding of scientific and technical information. Familiarity with regulatory affairs software and databases is also beneficial. Relevant certifications such as the Regulatory Affairs Certification (RAC) from the Regulatory Affairs Professionals Society (RAPS) are often preferred by employers. Prior roles that can lead to a career as a Regulatory Affairs Specialist include Quality Control Analyst, Product Development Scientist, or Compliance Officer.
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Demographic Data for Apopka, FL
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Quality Systems Engineer Online Courses and Training Opportunities
Salary for Quality Systems Engineer Jobs in Apopka, FL
Required or preferred licenses and certifications for Quality Systems Engineer positions.
Highest Education Level
Quality Systems Engineers in Apopka, FL offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Quality Systems Engineer position
- Product Lifecycle Management
- Internal Audits
- Supplier Quality
- Quality Systems
- Quality Management Systems
- Production Part Approval Process
- IATF 16949
- AS9100
- Control Plans
- Quality Engineering
- Advanced Product Quality Planning
- ISO 9001
- Metrology
- Corrective Actions & Preventive Actions
- ISO 13485
- Change Control
- Workplace Safety
- Failure Mode Effects Analysis
- Quality Management
- Statistical Process Control
- Manufacturing Engineering
- Minitab
- Process Controls
- Document Control
- Validation
- Good Manufacturing Practices
- Medical Device Sales
- FDA Regulations
- Document Management
- Root Cause Analysis
- Complaint Resolution
- Supply Chain
- Lean Six Sigma
- Engineering
- Continuous Improvement
- Six Sigma
- Product Development
- Quality Assurance
- Process Improvement
- Implementation
- Military Background
- Auditing
- Investigation
- Documentation
- Collaboration
- Reporting
- Bachelor's Degree
- Regulations
- Project Management
- Problem Solving
- Staff Supervision
- Organization
- Scheduling
- Leadership
- Communication Skills
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