Job Description

We are looking for a skilled Computer System Validation (CSV) Specialist to join our team. In this role, you will focus on assisting our clients in validating quality management system (QMS) software within the life sciences industry. You will ensure that the QMS software solutions meet regulatory requirements and industry standards, supporting our clients in achieving compliance with Good Manufacturing Practices (GMP), FDA, EMA, and other applicable regulations.

This is a client-facing role that requires strong technical expertise, regulatory knowledge, and excellent communication skills.

The Core Responsibilities For The Job Include The Following

System Validation Support for Clients:

  • Lead the validation of QMS software for clients, including planning, execution, and documentation of validation activities.
  • Develop and review validation deliverables such as Validation Plans (VP), User Requirement Sp...

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