Job description:

CSV Validation Engineer – Pharma Project

Company: Instrumentation and Control Solutions (ICS)

Location: Nashik, Aurangabad

Experience: 1–5 years

Notice Period: Immediate to 30 days preferred

Job Description

Instrumentation and Control Solutions (ICS) is seeking a CSV Validation Engineer for our pharmaceutical project in Mumbai. The ideal candidate will have strong experience in Computer System Validation within a regulated GxP environment and be familiar with industry guidelines such as GAMP5 and 21 CFR Part 11.

Key Responsibilities

• Prepare and execute validation deliverables in accordance with GAMP5 and 21 CFR Part 11.
• Perform IQ/OQ/PQ and validation of manufacturing systems (SCADA, HMI, PLC).
• Conduct and document CSV activities for pharmaceutical/life sciences systems.
• Ensure compliance with GxP standards and regulatory requirements.
• Collaborate with cross-functional teams in a regulated environment.

Required Skills & Experience

• 2–5 years of experience in CSV within pharmaceutical or life sciences projects.
• Hands-on knowledge of GAMP, 21 CFR Part 11, GxP, IQ/OQ/PQ.
• Prior experience with regulated GxP systems is mandatory.
• Strong documentation and compliance skills.

Benefits

• Competitive salary based on experience.
• Opportunity to work on high-impact pharma projects.
• Collaborative and supportive work environment.

How to Apply

Send your updated CV to: hr@ics-india.co.in

WhatsApp/Call: +91 91091 88709