Consultant–Computer System Validation-Life Sciences

Job description Consultant– Computer System Validation- Life SciencesWe are looking for smart, self-driven, high-energy people with intellectual curiosity and passion for excellence; specifically, we are looking for candidates at Consultant level who are experienced in IT Computerized System Validation (CSV) within Life Sciences domain.Responsibilities:Create, review, and approve validation deliverablesDefine IT system development processes (build, test, deploy, monitor) following Agile ways of working and ensure followed compliance in each release /IterationWorking experience on Agile/JIRA, Confluence, ALM Author major project validation deliverables as per client’s standard operating procedures Review and approve system lifecycle deliverables generated by project teamGuide project teams on applicable validation, security, and project management deliverablesAdvise project team on implementation of compliance and security control requirements at the appropriate stages of system developmentContribute to internal and external audits, assessments, or inspectionsEscalate critical compliance findings, risks, or issues into appropriate client unitsPrepare management reports regarding compliance operations and progressBasic Skills & Experience3 plus 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 validation deliverables.Knowledge of risk management processes.Thorough knowledge in compliance and validation concepts.Proven ability in supporting multiple projects, responding quickly to changing situations in complex environments.Preferable IT background to understand complexities on the program.Collaborative attitude.Location: New York, New Jersey, IndianapolisCandidates authorized to work for any employer in US without employer-based visa sponsorship are welcome to apply.

Infosys is unable to provide immigration sponsorship for this role at this timeRequired Skills & ExperienceStrong understanding of pharmaceutical compliance regulations and validation concepts.Experience with Agile and Waterfall methodologies.Familiarity with tools like ServiceNow, JIRA, Veeva, HPALM.Ability to manage multiple projects and adapt to complex environments.IT background preferred to understand program complexities.Excellent communication and collaboration skills.For candidates based out of NY,NJ states, estimated annual compensation will be $ to $Along with competitive pay, as a full-time Infosys employee you are also eligible for the following benefits :-Medical/Dental/Vision/Life Insurance Long-term/Short-term Disability Health and Dependent Care Reimbursement AccountsInsurance (Accident, Critical Illness, Hospital Indemnity, Legal) (k) plan and contributions dependent on salary level Paid holidays plus Paid Time Off EEO Infosys provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability.

Infosys provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability.