Edith Ruiz Email & Phone Number

Glendora, California, United States

Santa Fe Springs, California, United States

- Reviewing documents for accuracy, completeness, and compliance with standards and regulations.- Developing and implementing quality assurance processes for document production.- Maintaining document control systems and ensuring the security and integrity of documentation.- Organizing and managing documentation in a systematic and efficient manner.- Collaborating with cross-functional teams to ensure document quality and accuracy.- Identifying and addressing document-related issues and implementing solutions to improve processes.- Training and supporting team members on document quality and compliance standards- Developing and implementing quality assurance processes to ensure product quality and compliance with standards and regulations.- Conducting audits and inspections to identify areas for improvement and ensure adherence to quality standards.- Analyzing data and performance metrics to identify trends and areas for improvement - Collaborating with cross-functional teams to address quality issues and implement solutions. - Providing training and support to team members on quality standards and best practices.- Documenting and reporting quality issues and corrective actions.- Participating in the development and implementation of quality improvement initiatives.- Review and approve manufacturing labels, batch records, and incoming inspections.- Review and assist with non-conformances and CAPAs and help with the investigation.

Santa Fe Springs, California, United States

Oversee document control processes to ensure the accuracy, integrity, and compliance of critical documents within the biotech company.Establish and maintain document management systems, ensuring proper version control, distribution, and accessibility for relevant stakeholders.Collaborate with cross-functional teams to streamline document workflows, reducing processing times and improving overall efficiency.Implement and enforce document control policies and procedures in accordance with regulatory requirements, maintaining a high standard of quality and audit readiness.Conduct regular reviews and updates of documentation systems, staying abreast of industry best practices and contributing to continuous improvement initiatives.

Santa Fe Springs, California, United States

Reviewed quality control tests and inspections to ensure adherence to regulatory standards and product specifications.Collaborate with cross-functional teams to identify and address potential bottlenecks in quality processes.Analyze data and contribute to the implementation of effective quality management systems.Gain hands-on experience in a dynamic biotech environment, actively participating in initiatives to enhance overall product quality and compliance.

Project: End-to-end Clinical Supply Chain

Los Angeles, California, United States

Willowbrook, Ca

Master Of Science In Physician Associate Studies

Master Of Business And Science

Postgraduate Degree, Pre-Medicine/Pre-Medical Studies

Bachelor Of Science - Bs, Public Health