Process Validation Engineer

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

Description The Senior Manager of Validation Engineering is responsible for understanding and implementing validation requirements for a sterile injectables manufacturing and packaging facility. The ideal candidate has practical experience in qualification and validation as well as leadership experience. The Senior Manager of Validation Engineering will partner with internal and external customers to meet the needs of client projects, capital expansion projects, and maintenance of the validated

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

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