Senior Test Engineer
2 weeks ago
The position
As a Test Engineer, your role is critical in ensuring that all tests and procedures meet Standard Operations Procedures (SOP) and industry standards. You will also be responsible for performing testing on post-go-live changes, such as protocol amendments, Change Requests, and Technical Configuration Changes on the EDC system. Additionally, you will collaborate with CDP-EDC on queries related to test procedures. Your responsibilities include ensuring the smooth execution of these tasks to maintain the integrity and efficiency of the systems and processes As a Test Engineer at Novo Nordisk, you will have the opportunity to: Ensure that all tests and procedures meet Standard Operation ns Procedures (SOP) and industry standards. Perform testing on post-go-live changes such as protocol amendments, Change Requests, and Technical Configuration Changes on the EDC system. Collaborate with CDP-EDC on queries on test procedures. Perform various tasks related to Testing and Validation. Test inform build systems before production goes live to ensure smooth data flow and transformations. Provide detailed descriptions of scenarios that failed in the UAT plan and suggest additional test scenarios to be added to the Test Plan. Communicate suggestions or concerns regarding testing with relevant Clinical Data Programmer-EDC. Qualifications: To be successful in this role, you should have the following qualifications: MSc / BSc in Life Science or comparable degree in computer science, Information Technology clinical information management, or equivalent qualifications. 3+ years of experience in the pharmaceutical industry, preferably 1 year within clinical systems. Good knowledge of GxP guidelines within drug development. Understanding of clinical data types and specifications. Regular experience with communication and presentations. Personality with team spirit & self-motivation. About the Department : The Data Systems & Automation (DSA), Data Management team in Bengaluru is a highly competent and diverse team of professionals. We are responsible for providing functional and system support to execute clinical trials across our Product Development Plan portfolio. Our team has a strong understanding of Clinical Systems and interfaces, with a focus on the standardization of data flow across systems. We use Electronic Case Report Form (ECRF) development tools and know Clinical Data Interchange Standards Consortium (CDISC) concepts to aid CDISC submission, which is a mandate from regulatory authorities. Working at Novo Nordisk Novo Nordisk is a leading global healthcare company with a -year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63, employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we’re working toward something bigger than ourselves, and it’s a collective effort. Join us Together, we go further. Together, we’re life-changing.
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