Job Description:
- A day in the life of an Infoscion
- As part of the Infosys consulting team your primary role would be to actively aid the consulting team in different phases of the project including problem definition effort estimation diagnosis solution generation and design and deployment
- You will explore the alternatives to the recommended solutions based on research that includes literature surveys information available in public domains vendor evaluation information etc
- and build POCs
- You will create requirement specifications from the business needs define the to be processes and detailed functional designs based on requirements
- You will support configuring solution requirements on the products understand if any issues diagnose the root cause of such issues seek clarifications and then identify and shortlist solution alternatives
- You will also 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
Key Responsibilities:
- Key components of the responsibilities are as mentioned below but not limited to
- 5 yrs
- of Professional experience and strong knowledge with real time experience in IT Quality Compliance Computer System Validation Software Testing System Implementation in the Life Sciences industry
- Leads the effort to manage and or maintains validation of the GxP computerized systems
- Create Validation Plan Validation Report and Reviews validation documents such as URS FS FRA DD IQ OQ PQ s TRM
- Assure compliance with GxP GMP GCP GLP privacy requirements
- Develops and maintains IT GxP compliance documentation
- Ensure GxP Computerized Systems are validated as per GAMP 5 requirements
- Stakeholder management and good executor with required communication
- Candidate must have fair conceptual understanding on below key areas
- o IT QMS
- o Validation Qualification
- o Risk management
- o Handling of defects Deviations
- o Investigations
- o CAPA Handling
- o Test Management Compliance
- Candidate must have understating on latest regulations i
- e
- 21CFR Part 11 EU annex 11 and Guidelines e
- g
- GAMP5 guide
- Candidate will provide an application validation expertise practically on different scenarios as applicable case to case i
- e
- standalone enterprise etc
Technical Requirements:
- Primary skills Domain LifeSciences LifeSciences ALL
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
- 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
Preferred Skills:
Domain->LifeSciences->Pharma Regulations->Computer Systems Validation (CSV)
