Jeannette Ortiz Ayala
Quality/Compliance professional with experience in QMS for medical device and pharma industries. Proven in driving compliance, continuous improvement, ops. efficiency, and cross-functional team collaboration.
- Role
- Supplier Quality Manager at Essity
- Location
- Charlotte, NC, US
- LinkedIn followers
- 500 followers
About Jeannette Ortiz Ayala
Quality and Compliance professional with extensive experience in developing and implementing Quality Systems within the Medical Device and Pharmaceutical industries. Demonstrated leadership in QA/QS, driving continuous improvement, operational efficiency, and team productivity through strategic planning and cross-functional collaboration. Proven track record of delivering innovative solutions that enhance organizational performance while maintaining high-quality standards. Committed to leveraging strong problem-solving skills and adaptability to overcome challenges in dynamic environments.
Experience
Supplier Quality Manager
Apr 2025 — Present · Charlotte, NC, US
Manage the US LM SQM program. Define and implement process improvements to enhance compliance.• Ensure that product specifications/requirements are validated and met to confirm conformance.• Manage supplier qualification and performance monitoring process. Lead supplier audits.• Lead suppliers’ investigations and complaints to the appropriate root cause and effective corrective actions.• Management of the Distribution Center quality processes.
Education
University of Phoenix
Master of Business Administration, Technology Management
Universidad de Puerto Rico
Bachelor's degree, Chemistry
1992 — 1997
Universidad de Puerto Rico
Bachelor's Degree, Chemistry
University of Phoenix, Guaynabo, PR
Master of Business Administration - MBA, Technology Management
Skills
- Analytic Thinking
- Regulatory Analysis
- Six Sigma
- Quality Auditing
- Statistical Data Analysis
- Regulatory Policy
- Computer Proficiency
- Bilingual
- Compliance
- Team Leadership
- Medical Devices
- Capa
- Regulatory Requirements
- Quality Investigations
- Regulatory Documentation
- Pharmaceutical Industry
- Fda
- Technical Writing
- Quality Control
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