Quality Assurance Head for Pharmaceutical

HRTX; Mimaropa; On-site; PHP 1,800,000 - 2,400,000; Full time

Job summary

HRTX in Laguna is seeking a Quality Assurance Head for its Pharmaceutical Division. The role leads QA, ensures compliance with regulatory, safety, and quality standards, and oversees quality systems, audits, and documentation.

The position emphasizes team leadership and cross-functional collaboration to maintain product quality. Responsibilities include developing QA policies, conducting internal audits, supporting regulatory inspections, and driving continuous improvement across production,

Qualifications

• Bachelor's degree in Pharmacy, Chemistry or related field.
• Minimum of 710 years of QA experience in the pharmaceutical industry, with at least 3 years in a leadership role.
• Strong knowledge of GMP, FDA regulations, and quality management systems.
• Excellent leadership, communication, and analytical skills.

Responsibilities

• Lead and manage the QA team, ensuring effective implementation of quality management systems.
• Develop, review, and enforce QA policies, SOPs, and GMP compliance.
• Conduct internal audits and support external regulatory inspections.
• Monitor deviations, CAPA, change controls, and batch record approvals.
• Ensure cross-functional collaboration with Production, R&D, and Supply Chain for quality compliance.
• Implement continuous improvement initiatives to enhance product quality and operational efficiency.
• Provide training and guidance on quality standards and regulatory compliance.

Skills

QA leadership

GMP knowledge

FDA regulations

Audits

CAPA

Documentation

Cross-functional collaboration

Training

Education

Bachelor's degree in Pharmacy, Chemistry, or related field

Job description

Position Title: Quality Assurance (QA) Head Pharmaceutical Division
Work Location: Laguna
Work Schedule: Monday to Friday, Morning Shift
Employment Type: Full-Time

Job Purpose

The QA Head is responsible for leading the Quality Assurance function in the pharmaceutical division, ensuring compliance with all regulatory, safety, and quality standards. This role oversees quality systems, audits, documentation, and team management, guaranteeing that products meet both local and international standards.

Key Responsibilities

• Lead and manage the QA team, ensuring effective implementation of quality management systems.
• Develop, review, and enforce QA policies, SOPs, and GMP compliance.
• Conduct internal audits and support external regulatory inspections.
• Monitor deviations, CAPA, change controls, and batch record approvals.
• Ensure cross-functional collaboration with Production, R&D, and Supply Chain for quality compliance.
• Implement continuous improvement initiatives to enhance product quality and operational efficiency.
• Provide training and guidance on quality standards and regulatory compliance.

Qualifications & Requirements

• Bachelors degree in Pharmacy, Chemistry, or related field.
• Minimum of 710 years of QA experience in the pharmaceutical industry, with at least 3 years in a leadership role.
• Strong knowledge of GMP, FDA regulations, and quality management systems.
• Excellent leadership, communication, and analytical skills