Computer Systems Quality Assurance (CSQA)

Position : Computer Systems Quality Assurance (CSQA) Location: Indianapolis, IN (Hybrid) Duration: 12+ Months Contract Must Have Skills:IT CSV Validation of IT systems IT QA / QA eCompliance ManagerExperience with Veeva Quality Docs, ServiceNow, JIRA and HP ALMPharma industry experience is mandatoryMedical device experience is good to haveTotal Yrs. of Experience: Upto 12 yearsRelevant Yrs. of experience: 7 to 12 yearsDomain: Life Science (Preferred)

Roles & Responsibilities: Author equipment qualification and validation packages Plan coordination with equipment manufacturer or supplier for preventative maintenance Technical review and execution of qualification/validation protocols Execution of CSV initiatives Apply knowledge of quality principles, GMPs, federal regulations and standard procedures to deliverables Initiate CSV change controls on equipment Experience: Experience Required: 2-4 Years Experience in executing equipment validati

Description INCOG BioPharma is seeking a highly motivated Senior Validation Engineer with validation expertise to join our team. The Senior Validation Engineer is a key individual contributor role within the INCOG BioPharma Validation Department. The Senior Validation Engineer is responsible for understanding and implementing validation requirements for a sterile injectables manufacturing facility. The ideal candidate has subject matter expertise and practical experience in qualification and va

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but i