Associate Business Analyst | MBA Job Openings in Bangalore – Novo Nordisk Careers

Job Id: 20200810021

Company: Novo Nordisk

Job Role: Associate Business Analyst – Validation Engineer

Experience: 2+ Years

Qualification: Graduate

Job Location: Bangalore

Salary: Best in Industry

Vacancies: Not Mentioned

Website: www.novonordisk.com

Job Description Novo Nordisk Careers Job Openings in Bangalore Hiring For Associate Business Analyst in August 2020:

The holder of the position will be directly responsible for performing various tasks related to Computerised System Validation (CSV) which includes compliance related tasks and stakeholder management as a part of delivering services involving multiple stake holders with diverse interests, knowledge, cultural background and personality. You will have to develop plans, execute the services with acceptable service evaluations and manage test executioner reporting. You should also be able to perform Corrective Actions and Preventive Actions (CAPA) using 5x Why approach or any similar approach, provide compliance consulting for the IT projects, deliver compliance deliverables with respect to CSV and manage multiple concurrent tasks and be flexible.

Below skills are required

We expect you to hold a B,Tech, BE, MCA, M.Sc., B.Sc. or similar Graduate degree in relevant field (IT, CSc) preferred to have knowledge about ITIL and ISO quality management certification with the following experience.
Minimum 4+ years of experience in working as an IT quality control performing end to end validation
Minimum 2+ years of experience in working in a service level based preferably in the IT Quality domain
Minimum 2+ years of practical GXP areas with exposure to regulatory affairs
Minimum 2+ years in performing RCAs, CAPA and any other relevant IT services
You will probably learn many things here, but some of the technical areas we need you to already be quite experienced with.

Excellence in CSV and compliance process understanding
Compliance with NN Quality Management system
Able to take up IT quality coordinator roles at various stages of IT project
Prepare Master Validation Plan/Report, Quality/Validation Plan/Report, IT Quality Risk Assessment and Qualification Protocol/Report
Prepare Review and approve the following validation documentation established under Novo Nordisk QMS
Functional and Technical Design Specifications below URS level, IQP/R, OQP/R, XQP/R, p-IQP/R, p-XQP/R etc
Provide guidance to the IT System Subject Matter Expert on questions related to Computer System Validation
Test execution and reporting
Perform end to end validation (Author, review and approve validation documents)
Collect information and author URS
Review and approve validation documents on behalf of QA
Work with multiple stakeholder and projects
Efficiently author/review IT Periodic Evaluation reports
Contribute towards achievement of project goals
Demonstrate Pro-activeness and ownership
Manage own time planning, multiple concurrent tasks, timely deliverables and be flexible
Communicate and involve relevant stakeholders
Enhancing good team spirit and high degree of knowledge sharing
Deliver specific services that fulfil productivity/cost/quality/Timeliness KPI Criteria for stakeholders
Develop plans, execute and deliver the services with acceptable service evaluations
Ensure stakeholders evaluations are acted upon
Keep all documentation on relevant services up to date
To regularly communicate with management on the service status on improvement activities

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