Regulatory & Clinical BA – Life Science Job opening in Infosys Limited, (Pune, Maharashtra)

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We got a new job details in Infosys Limited & they are Hiring Candidates for Regulatory & Clinical BA – Life Science

Job Details
Company Name :
Infosys Limited
Company Location :
Pune, Maharashtra
Job Position :
Regulatory & Clinical BA – Life Science
Job Category : Jobs in Pune

Job Description :
Responsibilities
A day in the life of an Infoscion • As part of the Infosys consulting team, your primary role would be to get to the heart of customer issues, diagnose problem areas, design innovative solutions and facilitate deployment resulting in client delight. • You will develop a proposal by owning parts of the proposal document and by giving inputs in solution design based on areas of expertise. • You will plan the activities of configuration, configure the product as per the design, conduct conference room pilots and will assist in resolving any queries related to requirements and solution design • You will conduct solution/product demonstrations, POC/Proof of Technology workshops and prepare effort estimates which suit the customer budgetary requirements and are in line with organization’s financial guidelines • Actively lead small projects and contribute to unit-level and organizational initiatives with an objective of providing high quality value adding solutions to customers. If you think you fit right in to help our clients navigate their next in their digital transformation journey, this is the place for you!
Additional Responsibilities:
• Ability to develop value-creating strategies and models that enable clients to innovate, drive growth and increase their business profitability • Good knowledge on software configuration management systems • Awareness of latest technologies and Industry trends • PhD /Masters/ Bachelor’s Degree in Life sciences/Pharmaceutical Sciences from recognized universities or equivalent foreign degrees. • Expert in Pharmaceutical Regulatory Information Management landscape and systems in a pharmaceutical organization • Excellent knowledge in Regulatory Affairs Operation in global Pharmaceutical landscape • Good knowledge of business processes in EVMPD/IDMP /Product License Tracking (small molecules/Med devices/biologics)/CMC • Strong business consulting skills associated with engagement spanning over 6-18 months. Experience in SME and Consulting assignments in Regulatory area • Strong communication, Planning and Co-ordination skills and Stakeholder management • Good Knowledge of SDLC processes and must have performed requirement analysis, use case modeling, etc. from a business analysis/consulting standpoint. Hands on experience in creating managing SDLC process documentation and artifacts • Knowledge of vendors, products and solutions available in this area and expertise in some key products and solution • Logical thinking and problem solving skills along with an ability to collaborate • Understanding of the financial processes for various types of projects and the various pricing models available • Ability to assess the current processes, identify improvement areas and suggest the technology solutions • One or two industry domain knowledge • Client Interfacing skills • Project and Team management
Technical and Professional Requirements:
• Primary skills:Life Sciences – Regulatory Systems
Preferred Skills:
Life Sciences->Regulatory Systems
Educational Requirements
Bachelor of Engineering,Bachelor Of Technology,Bachelor Of Comp. Applications,Bachelor of Pharmacy,Master of Pharmacy,Master Of Technology,Master Of Comp. Applications

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