100% Remote. Option to go hybrid if close to site (ATO, AMA, ARI). EST preferred open to PST with minimum 4 hour overlap (8 6pm EST) IDEAL QUALIFICATIONS Bioprocessing/Pharmaceutical background preferred. Preference for candidates with previous experience in process development, clinical or commercial scale manufacturing with basic data science skills or an experience in

Assesses quality performance (or cost of quality) using statistical and analytical methods. Devises and implements various complex methods and procedures for inspecting, testing, and evaluating the precision, reliability, and accuracy of products, processes, and production equipment. Develops and establishes advanced quality systems and procedures, inspection plans, quali

Working collaboratively with multiple stakeholders such as R&D, manufacturing, supply chain, and quality to determine key design considerations for test equipment design, fabrication, and implementation. Exhibiting role model behavior of thorough engineering analysis and documentation. Executing projects from a basic concept to production, including developing specificati

Responsible for requirement"s analysis, test analysis, automated test procedure, test execution and maintenance of automation frameworks Responsible for verification strategy, infrastructure, planning and execution Will work with the Product Care (sustaining engineering) cross functional teams and lead testers to verify and validate software and automation hardware based

Engineers all end to end Material Flows from supplier receipt to lineside delivery in order to efficiently meet production requirements Developing a Plan for Every Part (PFEP) to document part numbers, quantities, suppliers, storage locations, part attributes, and replenishment plan Establish visual management process for the shop floor to align with the PFEP Update custo