Capgemini

GXP - Computerized System Validation | 6 to 9 years | Bangalore

Posted On

Feb. 5, 2025

Location

Bangalore, Karnataka

Experience Level

Experienced Professionals

Job Type

Permanent

Apply By

Feb. 26, 2025

Job Description

Choosing Capgemini means choosing a company where you will be empowered to shape your career in the way you’d like, where you’ll be supported and inspired by a collaborative community of colleagues around the world, and where you’ll be able to reimagine what’s possible. Join us and help the world’s leading organizations unlock the value of technology and build a more sustainable, more inclusive world.

Job Description

Ensure Review and Approval of planning, execution and documentation of Change Management Activities (at Asses / Review states); along with associated lifecycle documents and test documents for Change Lifecycle by maintaining the IT Compliance standards.
Responsible for the review and approval of Test Scripts and executed test cases to assure compliance with good documentation practices.
Individual contributor for Quality, Compliance, and Good Documentation Practices
Experienced in authoring & review of validation documentation such as URS, FRS, and SDS, Validation Plan, Issues Log, Design Review, IQ Protocol/Report, OQ Protocol/Report, Test Cases, Test executions, Trace Matrix, and Validation report, etc.
Working on Defect Management, CAPA and Deviation documentation, review and approval.
working on testing and validation management tools like ServiceNow, HP ALM, Document Management (GDRS/ EDMS), or equivalent tools, etc.
Research in supporting systems (e.g., GDRS, ServiceNow, EDMS, etc.) that store the records to be reviewed
Sign & Approve request forms for HPQC as IT Compliance approver.

Primary Skills

Ensure Review and Approval of planning, execution and documentation of Change Management Activities (at Asses / Review states); along with associated lifecycle documents and test documents for Change Lifecycle by maintaining the IT Compliance standards.
Working on Defect Management, CAPA and Deviation documentation, review and approval.
working on testing and validation management tools like ServiceNow, HP ALM, Document Management (GDRS/ EDMS), or equivalent tools, etc.

Secondary Skills

Responsible for the review and approval of Test Scripts and executed test cases to assure compliance with good documentation practices.
Experienced in authoring & review of validation documentation such as URS, FRS, and SDS, Validation Plan, Issues Log, Design Review, IQ Protocol/Report, OQ
Protocol/Report, Test Cases, Test executions, Trace Matrix, and Validation report, etc.
Research in supporting systems (e.g., GDRS, ServiceNow, EDMS, etc.) that store the records to be reviewed
Sign & Approve request forms for HPQC as IT Compliance approver.
Individual contributor for Quality, Compliance, and Good Documentation Practices

Capgemini is a global business and technology transformation partner, helping organizations to accelerate their dual transition to a digital and sustainable world, while creating tangible impact for enterprises and society. It is a responsible and diverse group of 340,000 team members in more than 50 countries. With its strong over 55-year heritage, Capgemini is trusted by its clients to unlock the value of technology to address the entire breadth of their business needs. It delivers end-to-end services and solutions leveraging strengths from strategy and design to engineering, all fuelled by its market leading capabilities in AI, cloud and data, combined with its deep industry expertise and partner ecosystem. The Group reported 2023 global revenues of €22.5 billion.

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