We are constantly looking to add to our core talent. If you are seeking a career that is challenging and rewarding, a work environment that is diverse and dynamic, look no further — Haemonetics is your employer of choice. Job Details Job Summary: This position is responsible to develop and implement changes to product design and/or to the automation and manufacturing process to achieve significant quality, or cost improvements. Requires participation in new product development programs, working with other business units to identify design-for-manufacturability issues, ensuring these issues are addressed prior to release, and mentoring engineers. Primary Responsibilities: Support manufacturing projects to ensure manufacturing success through cross-functional collaboration with other business units, coordination of overall project and budget management. Ensure that production processes and systems as well as our product designs for both existing and new products produce the highest possible quality (consistency) and lowest possible cost. Responsible for driving multiple improvement programs through to implementation and following-up on the results achieved, including: Quality Monitoring and Actions, Production Efficiency, Improve Assembly Methods, Document and Implement Approved Changes. Contribute to Lean/Six Sigma initiatives and Cost Improvement Projects, 5S, Kaizen events. Responsible for Non-Conforming Event (NCE) and Corrective and Preventive Action (CAPA) investigations and resolutions. May support new equipment and process validation activities (IQ/OQ/PQ). Qualifications: Required Bachelor's Degree Engineering. In lieu of an engineering degree, relevant Bachelor's degrees will be considered. Preferred, Master's Degree Engineering. Required, 0-3 years related experience in a manufacturing environment Preferred, reagent mixing and processing experience Preferred, medical device manufacturing experience Preferred, in-vitro diagnostics device manufacturing experience Candidate Skills: Design for Manufacturability Root Cause Analysis Statistical Analysis Technical Writing Medical Device Process Validation Licenses and Certifications: Knowledge of Six Sigma/Lean methods Preferred Green Belt or Black Belt Certification #LI-AR1 EEO Policy Statement Throughout our history, we have earned a solid reputation for product innovation, technical expertise, and operational excellence. Today, our products, internal research and development, marketing partnerships, and product acquisitions reflect our unwavering commitment to provide safe and available blood for patient transfusions and for use in pharmaceuticals. We rely on our talented global workforce to help us achieve our mission of providing innovative medical devices that advance the safety, quality, and availability of the world's blood supply. To achieve our business goals and objectives, we are committed to attracting and retaining the best and brightest talent while offering a challenging, dynamic, and exciting work environment that offers professional growth and development.