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 settings 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