This role involves working on validation and configuration tasks related to the Veeva Connector integrated with Compliance Wire, within a Life Sciences domain. The candidate will be responsible for ensuring GxP compliance through thorough validation documentation and planning.
Key Responsibilities
Develop and execute Veeva validation strategies including Test Plans and Validation Approaches.
Prepare and maintain validation documentation for the Compliance Wire / Veeva connector.
Configure and support the Veeva Connector setup.
Ensure compliance with GxP standards and regulatory requirements.
Collaborate with cross-functional teams to align validation efforts with business needs.
Familiarity with other Life Sciences platforms or tools.
Preferred Qualifications
Prior experience in the Life Sciences domain.
Hands-on experience with Veeva systems and Compliance Wire.
Understanding of regulatory environments and validation best practices.
Bachelor's or Master's degree in Life Sciences, Computer Science, or related field.
Works in the area of Software Engineering, which encompasses the development, maintenance and optimization of software solutions/applications.1. Applies scientific methods to analyse and solve software engineering problems.2. He/she is responsible for the development and application of software engineering practice and knowledge, in research, design, development and maintenance.3. His/her work requires the exercise of original thought and judgement and the ability to supervise the technical and administrative work of other software engineers.4. The software engineer builds skills and expertise of his/her software engineering discipline to reach standard software engineer skills expectations for the applicable role, as defined in Professional Communities.5. The software engineer collaborates and acts as team player with other software engineers and stakeholders.
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