Sr. Supplier Quality Engineer [SSQEAP426]

at Hologic, Inc. in Newark, Delaware, United States Job Description Hologic, Inc. has multiple openings in Newark, DE. Details are as shown below: JOB TITLE: Sr. Supplier Quality Engineer [SSQEAP426] WORKSITE: 600 Technology Drive. Newark, DE 19702 *No telecommuting. 25%-30% domestic travel required. WAGE RANGE: $124,238 - $186,600 annually JOB DESCRIPTION Execute all applicable activities to comply with regulatory standards and meet the requirements established in the Quality Management System around supplier's quality management. Conduct through technical reviews on Electronics/Metal suppliers to understand their capability to make Electronics/Metal materials. Oversee, assess, and monitor suppliers making parts as it relates to manufacturing, process and quality control practices, corrective action, continuous improvement, and First Article Inspection. Define and approve PPAP (Production Part Approval Process) requirement for all new and revised purchased parts (as applicable). Work with Post Market Surveillance and other applicable departments (Quality Engineering, MFG Engineering, Research and Development, etc.) to address complaints linked to Electronics/Metal situations. Resolve quality day-to-day issues associated with Electronics/Metal suppliers around the globe by addressing non-conformities. Update the ERP system with the status of the approved suppliers for the different Electronics/Metal materials. 25%-30% domestic travel required. MINIMUM REQUIREMENTS Master's degree or foreign equivalent in Mechanical Engineering, Electronic Engineering, Mechatronic Engineering, Industrial Engineering, or related field, and three (3) years of experience in the job offered or related. Alternatively, employer will accept a Bachelor's degree or foreign equivalent in Mechanical Engineering, Electronic Engineering, Mechatronic Engineering, Industrial Engineering, or related field, and five (5) years of experience in the job offered or related. SKILLS REQUIREMENTS Experience must include 3 years with the following: 1) Quality Assurance; 2) Supply Chain Operations; 3) Project Management; and 4) Production Part Approval Process (PPAP), supplier audits, or corrective action management. Experience must also include at least 6 months with the following: 5) Medical device manufacturing or a related industry; and 6) Regulatory standards and compliance in the medical device industry, such as FDA regulations (21 CFR), ISO 13485, or ISO 9001. Background checks may be required. APPLICANT INSTRUCTIONS: To apply, email resume to .... Must reference job title and job code. To view full details and how to apply, please login or create a Job Seeker account