Chemistry Jobs at Teva Pharmaceuticals | Apply Now for Analyst Role
Teva Pharmaceuticals is hiring a CSV Analyst at TAPI, Greater Noida, India. This is a unique opportunity to contribute to the validation and compliance of global R&D systems within the world’s leading supplier of Active Pharmaceutical Ingredients (APIs). With over 80 years of legacy and a presence across 13 international facilities, TAPI offers a collaborative environment where innovation meets purpose. Chemistry Jobs at Teva.
CSV Analyst – TAPI | Teva Careers
- Date: September 27, 2025
- Location: Greater Noida, India (201306)
- Job ID: 62216
Location of the Position
This opportunity is based at our advanced R&D center in Greater Noida, India.
The Opportunity
As a CSV Analyst, you will lead the validation of a new global ELN system for Teva’s R&D organization. From system design to global implementation, you will ensure compliance with GxP and regulatory standards while managing validation, maintenance, and change management for future system enhancements.
You will also support additional Computer System Validation (CSV) activities across TAPI sites, ensuring regulatory compliance and data integrity. Interested candidates, please apply for the Analyst Role.
How You’ll Spend Your Day
- Define Validation Plans, URS/FS/DS, Risk Assessments, and Testing Plans.
- Support PQ / UAT testing, Validation Summary Reports, and WI/SOP development.
- Conduct periodic reviews of laboratory applications for compliance with SDLC and data integrity controls.
- Document and monitor processes for data integrity, backup/restore, disaster recovery, and user management.
- Collaborate with stakeholders on business process discussions, compliance, and implementation.
- Document changes and new developments in accordance with GxP guidelines and good documentation practices.
Your Experience, Qualifications & Skills
- Degree in Computer Science, Chemistry, or related scientific/IT field.
- 2–5 years of experience in CSV within pharma/biotech.
- Strong knowledge of Pharma Laboratory Application Systems, user management, data integrity, backup/restore.
- Experience with software validations, HP gALM, and SDLC structure.
- Familiarity with GAMP5, 21 CFR Part 11, EU Annex 11, and GxP compliance.
- Knowledge of Windows OS, LAN/WAN, Servers, Switches, Routers.
- Proficiency in Microsoft Office and exposure to networked file systems.
- Strong documentation skills in Change Controls, CAPA, Deviations, and Investigations.
