2 jobs found

Reporting to the VP of Design & Development, the Quality Manager is responsible for maintaining the Quality Management System by updating and creating standard operating procedures, work instructions, and forms that comply with ISO-13485 and other standards. In addition, the Quality Manager will work with the R&D teams to create and approve quality and risk related specifications. Duties & Responsibilities: Drive key changes and continuous improvement in site Quality systems and procedures Liaise with other Design and Development sites within SteriPack to develop best QA practices Serve as the Quality engineer in programs, helping to create and/or review and sign quality related documents such as Design inputs, FMEAs, Hazard analysis, Trace Matrixes, Prints, Protocols, and Reports Serve as the Quality Management Representative during quality audits Respond to audit findings by creating and following through on action plans and CAPAs Assist in the...

At Boyd Technologies, we are experts in design & development, advanced manufacturing, and fulfillment operations for single-use devices and liquid media solutions. We are a small company with BIG goals. We believe in the power of people and value the importance of life outside of work. We are proud of our employee benefits and continually aspire to be a Best in Class workplace. We are growing our Process Engineering Team by adding a Sr. Process Engineer. This role will join a dynamic team of thinkers, doers and learners. Led by the VP of Quality & Engineering, the Sr. Process Engineer is responsible for the completion of machine setup, trials, and process qualifications for various medical devices and products in the single-use arena. They will work closely with the team to develop machine setups, tooling, and optimize equipment for production. The Sr. Process Engineer leads continual improvement efforts by analyzing workflow, space requirements, equipment layouts, and...