Grade-B Location-Hyderbad **Computer Systems Validation** Develop and maintain validation documentation in accordance with GxP, SDLC, and other regulatory requirements.

For LS_TQ&C; Consultant, based on the JD line you shared, the role is likely related to Life Sciences Technology, Quality & Compliance, with a robust focus on Computer Systems Validation (CSV).

Brief role explanation

The consultant would be responsible for ensuring that computerized systems used in regulated Life Sciences/Pharma environments are properly validated and compliant with GxP regulations.

Typical responsibilities could include:

- Preparing and maintaining CSV/validation documentation such as validation plans, requirements, test scripts, and validation reports.
- Ensuring systems follow GxP, SDLC, and regulatory requirements.
- Supporting system validation/testing, including reviewing test evidence and deviations.
- Performing or supporting risk assessments and compliance assessments.
- Working with IT, QA, business, and system teams during implementation, upgrades, and changes.
- Maintaining documentation required for audit and regulatory inspections.

📌 LS_TQ&C Consultant_Subcon (Hyderabad)
🏢 HORIGINE CONSULTING
📍 Hyderabad