CSV Engineer

Overview

Validate pharma computer systems per GAMP5 & 21 CFR Part 11.

Key Responsibilities

• validation
• gamp5
• cfr‑11
• csv
• pharma systems
• documentation

Tasks

-Preparation and execution of validation deliverables as per GAMP5 and 21 CFR Part 11 guidelines. -Conducting and documenting Computer System Validation (CSV) activities in pharmaceutical/life sciences environments.

Requirements

• gamp
• 21 cfr part 11
• gxp
• scada
• plc
• collaboration

What You Bring

-Strong ability to collaborate across cross-functional teams in a regulated setup. -Hands-on experience with GAMP, 21 CFR Part 11, GxP, IQ/OQ/PQ, and validation of manufacturing systems (SCADA, HMI, PLC, etc.). -Prior experience working with regulated GxP systems is essential. -Experience: Minimum 1 year (Pharma domain preferred) -Notice Period: Immediate joiners to 30 days

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About Instrumentation And Control Solutions

-As a specialist integrator, the company focuses on instrumentation, control systems, and HVAC solutions. -Engineers complete turnkey plant automation projects, including designing, installing, and commissioning PLC/DCS, SCADA, and instrumentation solutions. -Executes projects across sectors such as pharmaceutical manufacturing, breweries, food and beverage plants, distilleries, and commercial/industrial HVAC. -Authorized system integrator for Rockwell Automation (Allen‑Bradley), delivering custom PLC/DCS automation tailored to client needs. -Provides services like documentation, FDA‑compliant validation (21 CFR Part 11), NABL‑accredited calibration, and annual maintenance contracts. -Combines domain expertise in process industries with skilled technocrats to deliver end‑to‑end automation solutions.

Sector Specialisms