IT CSV / QA eCompliance Manager_Remote@Indianapolis,IN

Computer Systems Quality Assurance (CSQA) Location: Indianapolis, IN Onsite/EST Hours Duration: 12 Months Contract Experience: 7 12 Years Relevant Experience Please send your updated resume to me at pranayatburgeonitsdotcom Job Summary We are looking for a Computer Systems Quality Assurance (CSQA) / IT QA professional with strong IT Computer System Validation (CSV) experience in the Pharmaceutical/Life Sciences industry. The candidate will be responsible for validating IT systems and ensuring

Job Description: Seeking experienced CSV Engineers to provide onsite validation support within a regulated biopharmaceutical manufacturing environment. The primary focus of the position will be Computer System Validation, while also supporting equipment qualification and broader CQV activities as project priorities require. Consultants will support validation documentation and execution activities, assess computerized systems against GMP requirements, execute approved validation protocols, docum

Description INCOG BioPharma is seeking a highly motivated Principal Validation Engineer with commissioning and qualification of sterile manufacturing systems, combination packaging, or automation, computer system, and software assurance expertise to join our team. The Principal Validation Engineer is a key individual contributor role within the INCOG BioPharma Validation Department. The Principal Validation Engineer is responsible for understanding and implementing validation requirements for a

Job Title: Computer System Validation (CSV) Manager Work Location: Indianapolis, IN (Remote is fine for now) Contract duration: Long-term contract Visa: /Only Job Details: Mandatory Skills: - IT CSV Validation of IT systemsIT QA / QA eCompliance ManagerExperience with Veeva Quality Docs, ServiceNow, JIRA, and ALMPharma industry experience is mandatory.Medical device experience is good to have.Safety / PharmacovigilanceClinical trial management systemsGoogle Cloud Platform / GVP