Process Validation Engineer – Medical Devices (On-Site)

TERUMO (PHILIPPINES) CORPORATION; Quezon City; On-site; PHP 600,000 - 900,000; Full time

Job summary

TERUMO (PHILIPPINES) CORPORATION in Quezon City seeks a full-time Process Validation professional to plan, execute, and document validation activities for medical device manufacturing. You will prepare validation protocols and reports, analyze process data, identify risks, and recommend improvements to ensure product quality and regulatory compliance.

The role requires collaboration with production, engineering, and quality assurance on-site, and participation in audits and maintenance of

Qualifications

• Experience in process validation and validation for manufacturing processes and equipment.
• Knowledge of validation for systems supporting production and quality operations (CSV).
• Proficiency in quality control and quality assurance in regulated environments (medical device/pharma).
• Understanding of ISO 13485, FDA, GMP standards.
• Strong attention to detail and problem-solving; able to collaborate on-site with cross-functional teams.
• Excellent written and verbal communication in English.

Responsibilities

• Plan, execute, and document process validation activities for medical device manufacturing.
• Prepare validation protocols and reports; analyze data and identify process risks.
• Recommend improvements to enhance product quality and regulatory compliance.
• Collaborate with production, engineering, and quality assurance on-site.
• Participate in audits and maintain validation files.

Skills

Process Validation

Manufacturing validation

Process data analysis

Education

Bachelor's degree in engineering, life sciences, or related technical field

Tools

Computer System Validation

Job description

TERUMO (PHILIPPINES) CORPORATION in Quezon City seeks a full-time Process Validation professional to plan, execute, and document validation activities for medical device manufacturing. You will prepare validation protocols and reports, analyze process data, identify risks, and recommend improvements to ensure product quality and regulatory compliance.

The role requires collaboration with production, engineering, and quality assurance on-site, and participation in audits and maintenance of