CSV Engineer

INSTRUMENTATION AND CONTROL SOLUTIONS; Hyderabad; On-site; INR 500,000 - 800,000; Full time

Job summary

INSTRUMENTATION AND CONTROL SOLUTIONS is currently hiring a Computer System Validation (CSV) Engineer for a reputed Pharma organization with multiple locations including Hyderabad. The ideal candidate should have a minimum of 1 year experience in the Pharma domain, with hands-on experience in GAMP and 21 CFR Part 11.

Your responsibilities will include preparation and execution of validation deliverables, conducting CSV activities, and collaboration with cross-functional teams. Interested candidates should contact using the details provided.

Qualifications

• Minimum 1 year of experience in the Pharma domain.
• Hands-on experience with GAMP, 21 CFR Part 11, IQ/OQ/PQ.
• Prior experience working with regulated GxP systems.

Responsibilities

• Preparation and execution of validation deliverables as per GAMP5 and 21 CFR Part 11 guidelines.
• Conducting and documenting Computer System Validation (CSV) activities.
• Collaborating across cross-functional teams in a regulated setup.

Skills

CSV

21 CFR

IQ/OQ/PQ

Computer System Validation

GxP

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

Phone: [phone]

Email: [e-mail]