Director Site Quality

LDI Search LTD.; España; On-site; PHP 1,200,000 - 1,500,000; Full time

Job summary

LDI Search LTD. is seeking a Director of Site Quality in Romblon, España, who will take ownership of site quality strategy and regulatory compliance within the medical devices sector.

This role includes leading a quality organization and ensuring all products meet international regulatory standards, while influencing senior stakeholders to create a robust quality culture.

Qualifications

• Extensive quality leadership experience within medical devices.
• Strong track record in regulated manufacturing environments.
• Proven ability to drive quality culture, compliance excellence, and continuous improvement.

Responsibilities

• Lead and develop a high-performing quality organisation.
• Own the site quality strategy and QMS.
• Act as Quality Management Representative and influence senior stakeholders.

Skills

Quality leadership experience

Regulatory compliance

Continuous improvement

Job description

Overview

Director of Site Quality | Medical Devices

Director of Site Quality at a global leader in the medical devices sector, responsible for site quality strategy, regulatory compliance, and quality performance at a flagship manufacturing site.

Reporting to the Global Head of Quality, this role offers full ownership of site quality strategy, regulatory compliance, and quality performance within a complex, regulated environment. As Quality Management Representative, you’ll set direction for the QMS, influence senior stakeholders, and embed a strong, sustainable quality culture across the site.

Responsibilities

• Lead and develop a high-performing quality organisation; partner closely with Operations and Global functions to ensure products meet international regulatory standards.
• Own the site quality strategy and QMS; ensure regulatory compliance and quality performance within a highly regulated environment.
• Act as Quality Management Representative and influence senior stakeholders to embed a strong, sustainable quality culture across the site.

Qualifications

• Extensive quality leadership experience within medical devices.
• A strong track record in regulated manufacturing environments.
• Proven ability to drive quality culture, compliance excellence, and continuous improvement.