At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
Are You Ready to Create Your Own Sunshine?
As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a cooperative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”
Computer System Qualification & Validation (CSV)
- Ensure hardware qualification of computerized systems is completed as per approved protocols.
- Prepare, review, and execute qualification and validation documents for computerized systems and laboratory instruments.
- Perform and review software validation for new instruments in line with 21 CFR Part 11 requirements.
- Implement system and software validation for newly installed instruments/software.
2. Regulatory Compliance – 21 CFR Part 11
- Maintain and secure 21 CFR Part 11 compliance of laboratory instruments and equipment.
- Ensure compliance related to ERES, audit trails, software categorization, user and role management, and data security.
- Act as administrative rights holder for instrument and equipment software installed at SPML Baska.
3. System Administration & IT Support
- Preparation, review, and approval of System Administrator procedures for QC instrument software.
- Perform IT‑related activities as defined in instrument/equipment SOPs.
- Execute DTC‑related activities for the IT department.
- Monitor EDMS form due dates and system documentation lifecycle.
4. SOPs, Documentation & QMS
- Review, prepare, and maintain SOPs related to:
- Backup of electronic data
- System control policies
- IT infrastructure and system security
- Preparation, review, and approval of IT‑related protocols, policies, and documentation.
- Preparation, revi
📌 Executive IT (India)
🏢 Sun Pharmaceutical
📍 India
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