CSV Validation

Company Description

ICS is a leader in Automation, Instrumentation, and HVAC, providing turnkey solutions to clients. With in-house capabilities, ICS addresses the needs of process know-how, design and selection of instruments, and control systems (PLC/DCS). Our comprehensive services ensure seamless project execution for our clients.

Role Description

This is a full-time on-site role for a CSV Validation specialist located in Goa. The CSV Validation specialist will be responsible for conducting computer system validations, and ensuring all quality control and quality assurance standards are met. The specialist will work with various teams to ensure the validation processes align with regulatory and company standards.

Qualifications

✔️Strong skills in Computer System Validation.

✔️ Prepare and execute validation deliverables aligned with GAMP5 and 21 CFR Part 11 guidelines.

✔️ Perform IQ/OQ/PQ protocols for manufacturing systems such as SCADA, HMI, and PLC.

✔️ Conduct and document Computer System Validation (CSV) for regulated pharma and life sciences environments.

✔️Solid understanding of validation processes and regulatory requirements

✔️Excellent analytical and problem-solving skills

✔️Ability to work independently and collaborate with cross-functional teams

✔️Bachelor's degree in Engineering, Pharma or a related field

👥 Experience: 2– 4 years 📅 Join Date: Immediate joiners preferred-30days

📧 Send your resume to [recruitment@ics-india.co.in] or reach out via whtsapp- 9109188946 to explore the opportunity.