Test Engineer

2 weeks ago

Bengaluru, India Novo Nordisk AS Full time
Department: Data Systems & Automation (DSA)

Are you passionate about ensuring quality and compliance in the pharmaceutical industry? Do you have experience in testing and validation? We are looking for a Test Engineer to join our Data Systems & Automation (DSA), Data Management team in Bengaluru. If you are detail-oriented, have a strong understanding of clinical systems, and are ready for a new challenge, read on and apply today for a life-changing career.

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 processesAs 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.

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