We are currently hiring for the position ofComputer System Validation (CSV) Engineerin a reputedPharma organizationacross 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 perGAMP5and21 CFR Part 11guidelines.
- Hands-on experience withGAMP21 CFR Part 11GxPIQ/OQ/PQ and validation of manufacturing systems (SCADA HMI PLC etc.).
- Conducting and documentingComputer System Validation (CSV)activities in pharmaceutical/life sciences environments.
- Prior experience working withregulated GxP systemsis 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 yourpreferred location.
Contact:
Email:
Required Experience:
Junior IC
We are currently hiring for the position ofComputer System Validation (CSV) Engineerin a reputedPharma organizationacross multiple locations.Available Locations:Mandideep Nashik Goa Aurangabad Baddi Dabhasa Nagpur Hyderabad (Digwal) IndorePosition Details:Role:Computer System Validation (CSV...
We are currently hiring for the position ofComputer System Validation (CSV) Engineerin a reputedPharma organizationacross 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 perGAMP5and21 CFR Part 11guidelines.
- Hands-on experience withGAMP21 CFR Part 11GxPIQ/OQ/PQ and validation of manufacturing systems (SCADA HMI PLC etc.).
- Conducting and documentingComputer System Validation (CSV)activities in pharmaceutical/life sciences environments.
- Prior experience working withregulated GxP systemsis 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 yourpreferred location.
Contact:
Email:
Required Experience:
Junior IC
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