Infosys Consulting is looking for talented and highly motivated consultants to join our Life Sciences consulting practice. As a Senior Principal, you will work on strategic programs in the Life Sciences risk and compliance / advisory areas helping pharma, biopharma and medical devices companies develop strategic business capabilities while further deepening your knowledge in this area. • Lead Pre-Sales and Sales activities including Proposal Development, Solution and Value Proposition; in collaboration with larger Infosys teams, lead proposal development process; solution formulation; proposal pricing; client presentation; contract negotiations and deal closure • Engage and maintain contacts with key client stakeholders; proactively identify opportunities for business development, and lead workstreams to aid development of new business opportunities • Provide leadership in critical engagements and drive successful outcomes, and have ability to pursue and grow deep client relationships • Be a subject matter expert in areas such as Risk Management, Quality Management, Document Management, and Compliance Management • Understands how key risks and controls have an impact on the business from a pharma, business, operational and/or system perspective • Demonstrate a clear understanding of the risks and opportunities related to standard operating procedures and the governance policy framework • Makes recommendations for risk mitigation and audit strategies based on accurate identification of potential market, business, pharmaceutical, operational, IT and talent risks • Experienced with planning and conducting functional and domain specific risk assessment of Pharma and Medical Device programs / projects • Experienced in using industry wide risk management tools, and to perform root cause analysis on trends and address deviations via preventive, detective and corrective measures • Experience of working with Risk Management, Security and Compliance Policy frameworks, ISEC & Compliance, Records Management • Applies an understanding of company short-term and long-term strategic objectives and the risks that apply • Is knowledgeable about market and regulatory frameworks and trends that have the potential for substantive impact on organization strategies, policies, or risks • Knowledge and hands on experience conducting periodic or control assessment, audits and risk assessments • Knowledge of various validation tools and templates used throughout the Pharma and Medical Device industry • Participate in analyst meetings, industry speaking engagements, publish white papers/view points in leading industry journals • Participate in practice development activities; coach consultants; participate in consultant training and staffing processes • AI Risk Assurance • Successful track record using industry leading tools and techniques to conduct risk assessments and compliance checks to build digital solutions in a multi-disciplinary, multi-vendor corporate setting, and to validate assets • Experienced in leading strategic and tactical discussions with CxO level • Industry experiences working directly at pharmaceutical, medical devices or pharma distributor organization is a plus