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Work as Regulatory & Clinical BA at Infosys Limited

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Work as Regulatory and Clinical BA at Infosys Limited

Infosys Limited is an Indian multinational information technology company that provides business consulting, information technology and outsourcing services. The company was founded in Pune and is headquartered in Bangalore.

 Post : Regulatory & Clinical BA - Life Science

Job Description
• 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.

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

Candidate Profile
Master Of Comp. Applications,Master Of Technology, Master of Pharmacy, Bachelor of Pharmacy, Bachelor Of Comp. Applications,Bachelor Of Technology,Bachelor of Engineering

Additional Information
Experience : 5 Years and above
Qualification : M.Pharm, M.Sc
Location : Pune
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Regulatory Systems
End Date : 30th October, 2021


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