Quality Management Systems Leader – Build ISO‑9001 & FDA‑Ready

Grand Majesty Pharmaceutical Inc.; Cebu City; On-site; PHP 446,000 - 558,000; Full time

Benefits offered by this job

Competitive monthly salary ₱40,000–₱50

SSS, PhilHealth, Pag-IBIG, 13th month

Leave benefits

Leadership exposure to senior管理

Training and certification support

Job summary

Grand Majesty Pharmaceutical, Inc. in Cebu City is seeking a QMS Manager to build and lead the quality backbone of the business, ensuring processes are clear, documented, auditable, and compliant with ISO 9001, GDP, and Philippine FDA requirements.

You will design, implement, and maintain the QMS, map end-to-end processes, drive Lean/Six Sigma improvements, lead internal audits, CAPA closure, and prepare for FDA inspections, while coaching teams and aligning with stakeholders across operations,

Qualifications

• Bachelor-level degree in a relevant field with strong regulatory exposure.
• At least 5 years in quality management, process improvement, or internal audit.
• Experience with ISO 9001, GDP, FDA regulations preferred.

Responsibilities

• Design, implement, and maintain a QMS with auditable SOPs and records.
• Lead end-to-end process mapping and Kaizen or Six Sigma improvements.
• Run internal audits, manage CAPA, and prepare for FDA and customer audits.
• Coach staff on quality awareness and maintain supplier quality agreements.

Skills

Quality management

Process improvement

Internal audit

Lean Six Sigma

Regulatory compliance

Stakeholder management

Education

Bachelor’s degree in Pharmacy or related field

Tools

QMS software

MS Office

Document control systems

Job description

Grand Majesty Pharmaceutical, Inc. in Cebu City is seeking a QMS Manager to build and lead the quality backbone of the business, ensuring processes are clear, documented, auditable, and compliant with ISO 9001, GDP, and Philippine FDA requirements.

You will design, implement, and maintain the QMS, map end-to-end processes, drive Lean/Six Sigma improvements, lead internal audits, CAPA closure, and prepare for FDA inspections, while coaching teams and aligning with stakeholders across operations,