Chief Regulatory and Materials Officer (CRMO)

SV More Group; Quezon City; On-site; PHP 3,500,000 - 7,000,000; Full time

Job summary

S.V. More Group of Companies seeks an experienced Chief Regulatory and Materials Officer to provide executive leadership across Regulatory Affairs, Materials Management, Supply Chain, Warehouse, and Importation.

The CRMO will ensure regulatory compliance, product availability, inventory efficiency, and scalable operations for the group’s pharmaceutical and healthcare distribution activities. This strategic role requires deep expertise in FDA regulatory affairs, product registration, procurement,

Qualifications

• Bachelor of Science in Pharmacy (PRC licensed) is required.
• Minimum 15 years in the pharmaceutical industry.
• Minimum 10 years of management experience.
• Minimum 5 years of senior leadership experience.
• Strong and substantial experience in FDA Regulatory Affairs, Product Registration, Procurement, Forecasting and Supply Planning, Inventory Management, Warehousing, and Importation.

Responsibilities

• Lead Regulatory Affairs and Supply Chain Management strategy across the Group.
• Oversee FDA licensing, product registration, CPR renewals, variations, labeling, and regulatory compliance.
• Develop procurement, forecasting, supply planning, and inventory management strategies.
• Ensure inventory turns, aging, expiry prevention, dead stock reduction, and working capital efficiency.
• Oversee warehouse operations, storage compliance, GDP/GMP requirements, and importation activities.
• Build relationships with principals, manufacturers, and suppliers to ensure supply continuity.
• Lead S&OP and supply-demand alignment across functions.
• Identify and manage regulatory, supply, inventory, and operational risks.
• Provide executive analytics and strategic recommendations to the President and CEO.

Job description

S.V. More Group of Companies is looking for an experienced Chief Regulatory and Materials Officer (CRMO) to provide executive leadership across our Regulatory Affairs, Materials Management, Supply Chain, Warehouse, and Importation functions.

The CRMO will play a critical role in ensuring regulatory compliance, product availability, supply chain continuity, inventory efficiency, and operational scalability across the Group's pharmaceutical and healthcare distribution operations.

KEY RESPONSIBILITIES

• Lead and provide strategic direction for Regulatory Affairs and Supply Chain Management across the Group.
• Oversee FDA licensing, product registration, CPR renewals, variations, labeling, packaging, and regulatory compliance.
• Develop and oversee procurement, forecasting, supply planning, inventory, and materials management strategies.
• Ensure effective inventory management, including inventory turnover, aging, expiry prevention, dead stock reduction, and working capital efficiency.
• Oversee warehouse operations, inventory accuracy, storage compliance, productivity, and applicable GDP/GMP requirements.
• Lead importation and international supply activities, including import permits, customs coordination, shipment monitoring, and foreign supplier coordination.
• Build and maintain strategic relationships with principals, manufacturers, and suppliers to ensure supply continuity.
• Oversee new product launch readiness, product lifecycle management, and supply planning.
• Ensure packaging, artwork, labeling, and product information remain aligned with regulatory requirements.
• Lead cross-functional Sales and Operations Planning (S&OP) and supply-demand alignment.
• Identify and manage regulatory, supply, inventory, and operational risks.
• Lead supply chain improvement, digitalization, business continuity, and scalability initiatives.
• Provide executive-level analytics, performance reporting, and strategic recommendations to the President and CEO.

QUALIFICATIONS

• Bachelor of Science in Pharmacy
• Licensed Pharmacist (PRC) – required
• Minimum 15 years of experience in the pharmaceutical industry
• Minimum 10 years of management experience
• Minimum 5 years of senior leadership experience
• Strong and substantial experience in:
• FDA Regulatory Affairs
• Product Registration
• Procurement
• Forecasting and Supply Planning
• Inventory Management
• Warehousing
• Importation
• Pharmaceutical Distribution

PREFERRED QUALIFICATIONS

• MBA or Master's Degree in Supply Chain Management/Business Administration
• Regulatory Affairs Certification
• Supply Chain Certification

CORE COMPETENCIES

We are looking for a strategic and decisive leader with strong capabilities in:

• Enterprise and strategic thinking
• Regulatory governance and risk management
• Supply chain strategy and operational scalability
• Cross-functional leadership
• Crisis and stakeholder management
• Supply chain analytics and forecasting
• Working capital and inventory management
• Executive communication and talent development

WHY JOIN S.V. MORE GROUP OF COMPANIES?

Join a growing pharmaceutical and healthcare organization where you will have the opportunity to shape regulatory and supply chain strategy at the Group level, work with key internal and external stakeholders, and contribute to the continued growth and operational excellence of the organization.

If you have the experience, leadership background, and technical expertise to lead regulatory and supply chain functions in the pharmaceutical industry, we would like to hear from you.