Verified Job
Engineering - Architecture
CSV Engineer
Engineering - Architecture
#743059
Remote / WFH
INSTRUMENTATION AND CONTROL SOLUTIONS · Vadodara, Gujarat ·
Job Description
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
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
