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"Arcolab Hiring Computer System Validation (CSV) Professionals in Bangalore | Pharma IT Jobs 2026"
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"Arcolab Hiring Computer System Validation (CSV) Professionals in Bangalore | Pharma IT Jobs 2026."
(Arcolab Hiring Computer System Validation (CSV) Professionals in Bangalore)
Introduction:-
Arcolab, a well-known name in the pharmaceutical and life sciences domain, is currently hiring experienced professionals for Computer System Validation (CSV) roles at its Bangalore location. This opportunity is ideal for candidates who have hands-on experience with GxP-regulated IT systems, 21 CFR Part 11, EU Annex 11, and pharma IT operations.
With increasing regulatory focus on data integrity and validated computerized systems, CSV has become a highly in-demand skill in the pharmaceutical industry. Arcolab offers an excellent platform for professionals looking to strengthen their careers in pharma IT, validation, and compliance.
About Arcolab:-
Arcolab is a reputed pharmaceutical organization known for its strong compliance culture, quality-driven processes, and global regulatory standards. The company operates in regulated environments and follows strict GxP guidelines to ensure patient safety, data integrity, and product quality.
Working at Arcolab provides exposure to enterprise-level IT systems, regulated pharma environments, and international compliance standards, making it an attractive employer for validation and quality professionals.
Job Overview: Computer System Validation (CSV):-
Job Title:
Computer System Validation (CSV) Professional
Location:
Bangalore, India
Industry:
Pharmaceuticals / Life Sciences / Pharma IT
Experience Required:
2 to 10 Years
These roles focus on ensuring compliance, validation, and lifecycle management of enterprise systems used in regulated pharmaceutical environments.
Key Responsibilities:-
CSV Documentation & Execution:
Prepare, review, and execute CSV deliverables such as validation plans, risk assessments, IQ/OQ/PQ documentation, and summary reports for enterprise-level systems.
Regulatory Compliance:
Conduct and review 21 CFR Part 11 and EU Annex 11 compliance assessments for computerized systems, equipment, and instruments.
Risk Assessment & Periodic Review:
Perform risk assessments and periodic system reviews, including:
User access management
Error and event log review
Audit trail verification
QMS Event Management:
Manage and document QMS events such as deviations, change controls, CAPAs, and incidents in accordance with regulatory and internal quality requirements.
IT Operations Support:
Support regulated IT operations related to:
Data integrity and security
System backup and restoration
Controlled system maintenance activities
GxP Compliance Assurance:
Ensure continued compliance of GxP systems during enhancements, upgrades, and routine maintenance activities.
Required Qualifications:-
Candidates applying for Arcolab CSV roles should meet the following criteria:
The Computer System Validation roles at Arcolab in Bangalore offer a strong career opportunity for professionals looking to grow in pharma IT and compliance. With increasing regulatory expectations and digital transformation in pharmaceuticals, CSV professionals play a critical role in ensuring system reliability and patient safety.
If you have the right experience and are ready to work in a regulated, quality-focused environment, this opportunity at Arcolab should not be missed.
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