Life Sciences CSV Validation Consultant

Nnit A/S; Makati; Hybrid; PHP 600,000 - 1,000,000; Full time

Benefits offered by this job

Competitive Compensation

13th Month Pay

Performance Bonus (discretionary)

Rice Subsidy

HMO (Employee and Dependent)

Life Insurance

Vacation Leaves and Sick Leaves

Flexible Working Hours

Hybrid set up

Job summary

NNIT is seeking a Validation Consultant in Manila to ensure regulatory compliance and company CSV processes across Life Sciences IT projects, with a focus on data integrity and quality. You will prepare Validation Plans, Specifications and IQ/OQ/PQ documentation, support risk assessments, participate in E2E validations, and help drive quality improvements in a fast-paced, hybrid work environment.

This role emphasizes independent documentation, quality management, and collaboration with project

Qualifications

• 3+ years in a consultancy/quality role in Life Sciences IT
• Experience with validated computer systems (CSV), GxP and Quality Management
• Knowledge of the V-model/Agile delivery and ISPE GAMP5 guidelines
• Experience creating and reviewing validation documentation
• Life Sciences/biotech/pharma domain experience
• Strong verbal and written communication; ability to work independently and with teams
• Ability to operate in a dynamic environment with urgency and strong attention to detail

Responsibilities

• Act as Validation Consultant in small to medium Life Sciences IT projects
• Prepare validation documents independently (Plans, Specifications, IQ/OQ/PQ)
• Contribute to risk management activities and validation/test strategies
• Participate in end-to-end validations and ensure data integrity and compliance
• Review IT projects/docs to meet QMS process requirements
• Identify and implement process improvements

Skills

CSV

GxP

Risk management

Documentation

Tools

Kneat

ValGenesis

GAMP5 guidelines

Job description

NNIT is seeking a Validation Consultant in Manila to ensure regulatory compliance and company CSV processes across Life Sciences IT projects, with a focus on data integrity and quality. You will prepare Validation Plans, Specifications and IQ/OQ/PQ documentation, support risk assessments, participate in E2E validations, and help drive quality improvements in a fast-paced, hybrid work environment.

This role emphasizes independent documentation, quality management, and collaboration with project