Embark on a rewarding career as a Custom Software Engineer, where you will drive the design, development, and refinement of specialized software solutions. This role involves crafting high-performance components across various systems and applications, utilizing modern frameworks and agile methodologies to meet specific business needs. You will play a key part in delivering scalable, tailored solutions that address unique project requirements and business objectives.

Independently contribute as a Subject Matter Expert (SME) and actively participate in team discussions, offering solutions to complex work-related challenges. Collaborate with cross-functional teams to translate requirements into precise technical specifications. Maintain transparent communication with stakeholders, ensuring alignment on project goals and deliverables. Continuously assess and enhance application performance and reliability, while mentoring junior team members through knowledge sharing and best practice guidance.

Demonstrate proficiency in Data Analytics and Pharmacovigilance & Drug Safety Surveillance. Possess techno-functional expertise in Pharmacovigilance, particularly with LSMV Safety, database implementation, configuration, and production support using Java, SQL, SpringBoot, and REST APIs. Execute end-to-end LSMV deployment lifecycles, from requirement gathering to release management and hypercare support. Leverage strong SQL and Oracle skills for data validation and troubleshooting within regulated life sciences environments. Apply robust analytical and problem-solving skills to interpret complex data, generate insights, and address technical challenges. Experience in designing data-driven solutions and a solid understanding of data management principles are essential.