Life Sciences Management Consultant - (GRC)

Infosys; Bengaluru; On-site; INR 1,500,000 - 2,700,000; Full time

Job summary

Infosys Life Sciences (IC-LS) seeks experienced consultants for delivery in Bengaluru, India. The role focuses on regulatory compliance, validation execution, and risk management across IT projects in the pharma sector.

Candidates should understand 21 CFR Part 11, GxP, and GAMP 5, and have hands-on validation experience with ERP and QA systems. Ideal candidates bring domain knowledge in clinical or regulatory applications, plus strong communication and teamwork skills for global client

Qualifications

• Good communication skills and analytical thinking are required.
• Familiarity with validation concepts in IT projects and risk management.
• Experience with pharma compliance regulations like 21 CFR Part 11, GxP and GAMP 5.

Responsibilities

• Deliver business results for global health and life sciences clients.
• Serve as team member, track lead or engagement lead on consulting engagements.
• Execute engagements in global delivery model with cross-region consultants.
• Analyze problems and structure complex business analyses.
• Collaborate with cross functional client teams for gap analysis and improvements.
• Support multiple projects and respond to changing environments.

Skills

Communication skills

Analytical thinking

Tools

SAP

S/4HANA

Trackwise

QMS

DMS

Job description

• 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)

• 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)

We are looking for smart, self-driven, high-energy people with top-notch communication skills, intellectual curiosity and passion for excellence. Our analysts have a blend of in-depth domain expertise, strong analytical and conceptual thinking skills and excellent soft skills. We are looking for people who have demonstrated proven success in roles and through abilities in Computerized System Validation, Risk Management and Audits

At 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