Work Setup: Onsite (Makati)
Work Schedule: Monday to Friday (8am-5pm)
Responsibilities:
- Implement and monitor the Laboratory QMS in compliance with ISO 15189 DOH LTO and other relevant standards.
- Lead internal audits manage CAPA (Corrective and Preventive Actions) and support accreditation readiness (ISO/JCI).
- Develop and deliver training programs and competency assessments for laboratory staff.
- Coordinate EQA/PT programs and track performance and corrective actions.
- Support incident investigations and risk management activities to ensure continuous improvement.
- Prepare and submit QA dashboards reports and audit summaries to management.
Qualifications:
Education:
- Licensed Medical Technologist (PRC)
Experience / Knowledge:
- 3 to 5 years experience in a clinical laboratory with at least 2 years in QA compliance or training.
- Strong understanding of ISO 15189 DOH and JCI requirements. Skills:
- Skilled in audit management document control and staff development.
- Excellent analytical communication and documentation skills.
- Certifications in ISO 15189 Internal Auditing Quality Management or Training are an advantage.
- Excellent communication presentation and interpersonal skills
- Proficient in Microsoft Office and basic reporting tools
Traits:
- Empathetic professional proactive and results-oriented
- Calm under pressure and able to manage fast-paced clinical environments
- Passionate about service excellence continuous improvement and cross-functional collaboration
Work Setup: Onsite (Makati) Work Schedule: Monday to Friday (8am-5pm) Responsibilities: Implement and monitor the Laboratory QMS in compliance with ISO 15189 DOH LTO and other relevant standards.Lead internal audits manage CAPA (Corrective and Preventive Actions) and support accreditation readiness ...
Work Setup: Onsite (Makati)
Work Schedule: Monday to Friday (8am-5pm)
Responsibilities:
- Implement and monitor the Laboratory QMS in compliance with ISO 15189 DOH LTO and other relevant standards.
- Lead internal audits manage CAPA (Corrective and Preventive Actions) and support accreditation readiness (ISO/JCI).
- Develop and deliver training programs and competency assessments for laboratory staff.
- Coordinate EQA/PT programs and track performance and corrective actions.
- Support incident investigations and risk management activities to ensure continuous improvement.
- Prepare and submit QA dashboards reports and audit summaries to management.
Qualifications:
Education:
- Licensed Medical Technologist (PRC)
Experience / Knowledge:
- 3 to 5 years experience in a clinical laboratory with at least 2 years in QA compliance or training.
- Strong understanding of ISO 15189 DOH and JCI requirements. Skills:
- Skilled in audit management document control and staff development.
- Excellent analytical communication and documentation skills.
- Certifications in ISO 15189 Internal Auditing Quality Management or Training are an advantage.
- Excellent communication presentation and interpersonal skills
- Proficient in Microsoft Office and basic reporting tools
Traits:
- Empathetic professional proactive and results-oriented
- Calm under pressure and able to manage fast-paced clinical environments
- Passionate about service excellence continuous improvement and cross-functional collaboration
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