Consultant - Business Consulting (Life Science - CSV)
Infosys View all jobs
- Bangalore, Karnataka
- Permanent
- Full-time
We are looking for people who have demonstrated proven success in roles and through abilities in Computerized System Validation, Risk Management and AuditsAt IC-LS, you will:
- Be responsible for the delivery of business results to global health and life sciences clients.
- Serve as a team member, track lead or engagement lead on business consulting engagements for clients.
- Execute consulting engagements in a global delivery model, working with consultants across regions.
- Analyze problems, and structure complex business analyses.
- Work with cross functional client teams to perform gap analysis and identify improvement options.
- Effectively collaborate with the internal and external stakeholders.
- Participate in a variety of firm building events
- Knowledge of validation tools and templates used in the pharmaceutical industry.
- Proven ability in supporting multiple projects, responding quickly to changing situations in complex environments.
- Preferable IT background to understand complexities on the program.
- Experience in Agile and waterfall methodology
- Knowledge and hands on experience in conducting periodic or control maturity assessment and Audits
- Knowledge in Saas/Cloud Qualifications
- 4 - 14 years of professional experience in the Life Sciences industry working for a consulting services organization and/or industry.
- Good understanding of key pharmaceutical compliance regulations like 21 CFR Part 11, GxP and GAMP 5.
- Experience creating, reviewing and approving / acknowledging validation deliverables.
- Knowledge of risk management process and quality management requirements which assures that IT Projects meet Quality and Regulatory requirements
- Experience in validation of Enterprise applications such as SAP / S4 HANA projects, Trackwise, QMS, DMS and etc.
- Functional knowledge in any of the domain applications such as Clinical applications like EDC, CTMS etc., Regulatory applications like CDR, or any other applications/system used in Pharma industry.
- Thorough Knowledge in compliance and validation concepts. (Change, Deviation, Supplier management)