CSV Engineer

INSTRUMENTATION AND CONTROL SOLUTIONS

Solan

On-site

INR 500,000 - 800,000

Full time

14 days+

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Job summary

A reputed Pharma organization is hiring for the position of Computer System Validation Engineer. This role involves preparation and execution of validation deliverables, focusing on GAMP5 and 21 CFR Part 11 guidelines. Candidates should have a minimum of 1 year of experience in the Pharma domain and must be able to collaborate across cross-functional teams. Strong hands-on experience with GxP systems is essential. Interested candidates are encouraged to apply with their updated CV.

Qualifications

  • Minimum 1 year of experience in a Pharma domain.
  • Hands-on experience with validation of manufacturing systems.
  • Strong ability to collaborate across cross-functional teams.

Responsibilities

  • Preparation and execution of validation deliverables as per GAMP5 and 21 CFR Part 11 guidelines.
  • Conducting and documenting Computer System Validation activities in pharmaceutical environments.
  • Prior experience working with regulated GxP systems.

Skills

CSV
GAMP
21 CFR Part 11
GxP
IQ/OQ/PQ
SCADA
HMI
PLC

Job description

Skills:

CSV, 21 CFR, IQ, OQ, PQ, Computer System Validation,

We are currently hiring for the position of Computer System Validation (CSV) Engineer in a reputed Pharma organization across multiple locations.

Available Locations:
  • Mandideep
  • Nashik
  • Goa
  • Aurangabad
  • Baddi
  • Dabhasa
  • Nagpur
  • Hyderabad (Digwal)
  • Indore
Position Details:
  • Role: Computer System Validation (CSV) Engineer
  • Industry: Pharma
  • Experience: Minimum 1 year (Pharma domain preferred)
  • Notice Period: Immediate joiners to 30 days
Key Responsibilities & Skills:
  • Preparation and execution of validation deliverables as per GAMP5 and 21 CFR Part 11 guidelines.
  • Hands‑on experience with GAMP, 21 CFR Part 11, GxP, IQ/OQ/PQ, and validation of manufacturing systems (SCADA, HMI, PLC, etc.).
  • Conducting and documenting Computer System Validation (CSV) activities in pharmaceutical/life sciences environments.
  • Prior experience working with regulated GxP systems is essential.
  • Strong ability to collaborate across cross‑functional teams in a regulated setup.

If you meet the above requirements and are interested in this opportunity, please share your updated CV mentioning your preferred location.

Contact: 9109188512

Email: ankur.tiwari@ics-india.co.in

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