L1 & L2 support Engineer for Veeva Vault QMS Capgemini

5.0 - 9.0 years

0 Lacs

pune, maharashtra

On-site

You will be responsible for: - Providing L1 & L2 support for Veeva Vault QMS, QualityDocs, and Training, resolving user issues and system errors. - Troubleshooting workflow automation, document control, access management, and security concerns. - Collaborating with IT teams to resolve integration, database, and system performance issues. - Liaising with Veeva Support for system updates, issue escalations, and troubleshooting. - Maintaining Veeva Vault applications ensuring system stability, performance, and compliance. - Managing user roles, permissions, and security policies to control data access. - Performing software updates, patches, and configurations in compliance with validation requ...

Posted 23 hours ago

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Validation Compliances Gxp Consultant (On-Site) QAAgility Technologies

8.0 - 12.0 years

0 Lacs

karnataka

On-site

Job Summary: You will be responsible for overseeing and managing the validation processes of systems, processes, or products to ensure compliance with industry standards and regulations. Your role will involve extensive experience in system validation, quality assurance, and compliance management, with a focus on meeting regulatory requirements and ensuring operational efficiency. Key Responsibilities: - Lead and manage system validation activities for projects to ensure compliance with relevant regulatory standards such as FDA, GMP, ISO, and 21 CFR Part 11. - Develop and execute validation plans, protocols (IQ, OQ, PQ), and reports for systems and processes. - Coordinate with cross-function...

Posted 1 month ago

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Validation Compliances Gxp Consultant QAAgility Technologies

8.0 - 12.0 years

0 Lacs

karnataka

On-site

Job Summary: As a Validation Compliance GxP Consultant, you will be responsible for overseeing and managing the validation processes of systems, processes, or products to ensure compliance with industry standards and regulations. You should have extensive experience in system validation, quality assurance, and compliance management, with a focus on meeting regulatory requirements and operational efficiency. Key Responsibilities: You will lead and manage system validation activities for projects to comply with regulatory standards such as FDA, GMP, ISO, and 21 CFR Part 11. Developing and executing validation plans, protocols (IQ, OQ, PQ), and reports for systems and processes is a key part of...

Posted 2 months ago

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Adobe Sign Teamware Solutions

2.0 - 4.0 years

2 - 6 Lacs

Hyderabad, Telangana, India

On-site

Teamware Solutions is seeking a proficient Adobe Sign Specialist to integrate and optimize electronic signature workflows within our business processes. You'll play a crucial role in enabling secure, efficient, and legally compliant digital document signing, streamlining operations and enhancing the user experience for various departments. Key Responsibilities Design, configure, and implement electronic signature workflows using Adobe Sign to meet specific business requirements. Integrate Adobe Sign with existing enterprise applications such as CRM (e.g., Salesforce), ERP, Microsoft SharePoint, and custom systems. Create and manage Adobe Sign templates, forms, and workflows , ensuring proper...

Posted 3 months ago

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