CSV Validation Consultant — Life Sciences (Hybrid)

Nnit A/S; Makati; Hybrid; PHP 700,000 - 900,000; Full time

Benefits offered by this job

Competitive compensation

13th month pay

Performance bonus

Rice subsidy

HMO for employee and dependents

Life insurance

Vacation and sick leaves

Emergency loan

Year-end gift

Wedding gift

First baby gift

Breakfast once a week

Fruits and pantry snacks

Flexible working hours

Hybrid setup

Job summary

NNIT is seeking a Validation Consultant to ensure regulatory compliance and CSV adherence within Life Sciences IT projects in the Philippines. You will prepare validation plans, specifications, and qualification documentation, and contribute to project milestones and risk management.

The role requires experience with validated systems, GxP, and ISPE GAMP5 guidance. You will work in a dynamic, team-based environment with strong emphasis on quality, data integrity, and timely delivery.

Qualifications

• At least 3 years in a consultant/quality role.
• Experience working with validated computer systems (CSV), GxP and Quality Management.
• Knowledge of the V-model/Agile delivery, ISPE GAMP5 guidelines.
• Experience creating and reviewing validation documents.

Responsibilities

• Act as Validation Consultant in Life Sciences IT projects, small to medium in complexity.
• Independently prepare validation documents (Plans, Specifications, Qualification docs).
• Support project milestones, reporting and risk management input.
• Contribute to CSV project activities including data integrity.
• Review IT project documentation to ensure process compliance with QMS.
• Identify and implement process improvements.
• Prepare IQ/OQ/PQ testing activities including deviation handling and reporting.

Skills

CSV validation

GxP knowledge

ISPE GAMP5

Documentation creation/review

Life Sciences/Pharma experience

Communication skills

Independence

Dynamic fast-paced work

Attention to detail

Job description

NNIT is seeking a Validation Consultant to ensure regulatory compliance and CSV adherence within Life Sciences IT projects in the Philippines. You will prepare validation plans, specifications, and qualification documentation, and contribute to project milestones and risk management.

The role requires experience with validated systems, GxP, and ISPE GAMP5 guidance. You will work in a dynamic, team-based environment with strong emphasis on quality, data integrity, and timely delivery.