Manager / Sr Manager- Veeva Vault Configuration and Admin Ocugen India Pvt Ltd

8.0 - 12.0 years

0 Lacs

hyderabad, telangana

On-site

As a Technical Configuration and System Integration Specialist, your role involves configuring Veeva Vault modules to meet business requirements and ensuring system validation. Additionally, you will be responsible for document management and system administration, specifically focusing on Quality Docs and Electronic Document Management System (EDMS). Key Responsibilities: - Administer and maintain Veeva Vault DMS, including Quality Docs and other modules. - Configure Vault modules such as Quality Docs, QMS, RIM, Promo Mats, and eTMF. - Oversee the document lifecycle from creation to archiving in compliance with GxP and quality standards. - Maintain version control, metadata, and audit readi...

Posted 1 day ago

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Health Information Technician Ti Steps

3.0 - 5.0 years

4 - 8 Lacs

hyderabad, telangana, india

On-site

Health Information Technician Roles and Responsibilities: Manage and organize health information data. Ensure the accuracy, accessibility, and security of patient records. Maintain patient confidentiality and comply with healthcare regulations. Assist in the implementation and management of health information systems. Collaborate with healthcare providers to ensure proper documentation. Required Skills: Knowledge of medical terminology Proficiency in health information systems Attention to detail Strong organizational skills Ability to maintain confidentiality

Posted 3 days 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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Visa Consultant ManageMy Vacations

2.0 - 6.0 years

0 Lacs

delhi

On-site

Role Overview: You will be a full-time Visa Consultant based in New Delhi, responsible for managing visa processing and immigration matters. Your role will involve consulting with clients to determine their visa requirements, preparing and submitting visa applications, tracking application statuses, and offering guidance on immigration policies. Additionally, you will maintain accurate records, liaise with authorities, and provide ongoing assistance to clients throughout the visa application journey. Key Responsibilities: - Consult with clients to understand their visa needs - Prepare and submit visa applications - Monitor and follow up on application statuses - Advise clients on immigration...

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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