At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. The Role The Quality Engineer (Supplier) in our Plymouth manufacturing location is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the fo

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. The Role The Senior Quality Engineer in our Eden Prairie facility is responsible for managing processes and leading projects to maintain and improve the quality system in accordance with the requirements of

The Quality Specialist is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. This role coordinates document control transactions, site record retention, calibration and inspection activities. In addition, the Quality Spe

The Quality Specialist is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. This role coordinates document control transactions, site record retention, calibration and inspection activities. In addition, the Quality Spe

The Senior Quality Engineer is responsible for managing processes and leading projects to maintain and improve the quality system in accordance with the requirements of, as appropriate, the following standards IS0 9001, ISO 13485, MDSAP and FDA 21 CFR Part 820/211, EU MDR and other applicable standards. This role leads complaint/CAPA investigations, supplier quality impro

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Quality Systems Engineer II LinkedIn Twitter Email Message Share Why Join Bracco Medical Technologies? We care as much about our employees as we do our patients. Our culture fosters a work environment where employees can thrive, be passionate and have fun along the way. Each member of the Bracco Medical Technologies team has the power to make a difference......every day!

Product Quality & Corrective Action process Support development & industrialization of the Nilfisk Product Quality reporting system and CA process Train & Coach personnel in the use of the Technical Failure Reporting (TFR) system, Train & Coach personnel in the 8D problem solving process and applicable quality tools such as (5W2H, Cause & effect diagrams), Foster a custom

Part Approval process and development through execution phases, to support current development of the product design and manufacturing supplier process. Part approval plan of PPAP and execution phases. Measurement plan for parts received during the design development & verification stages of the project. Plan to secure supplier process capability data on similar component

Quality Management System (30%) Develop and maintain control of calibration, verification of measuring equipment system, Support the organization to meet with the calibration, verification plan, Support internal product and process audits, (ISO 9001, Intertek ETL), Write product test procedures, work instructions, SOPs as required, Promote the use of continuous improvemen

Quality Management System Support Quality Management System (applicable ISO or internal standards), improvement and maintenance, including internal layered and process, system audits, Manage and coordinate internal, external audits to ensure compliance and certification, Support preparation and execution of Management Review Meetings with project overviews (NSD content),

Under minimal supervision of the VP of R&D, the Continuation Engineering Manager supervises, directs and coordinates activities of the continuation engineering personnel. This person acts as the primary contact for other departments to provide support regarding continuation engineering activities including but not limited to product quality, supplier related, margin impro

This position will provide full time environmental health and safety support to operations and will ensure that all practices are in compliance with Federal, State, Province, and local regulatory requirements. The position will be responsible for coordinating regulatory programs, permitting applications, lead the development and coordination of EHS training programs as re

Support compliance with all Local, State, and Federal Laws. Maintaining accurate daily, weekly, and monthly metrics, to report to the EHS manager and local Management team. Conduct Risk assessments related to jobs performed by employees and suggest risk mitigation strategies. Recommending and implementing appropriate risk mitigation measures to management. Training and as

Build Quality into all aspects of their work by maintaining compliance to all quality requirements. Preferred Qualifications 5 8 Years with BS, 3 6 Years with MS, 0 3 Years with PhD Additional Preferred Job Specific Requirements 1. Strong MS Excel skills and knowledge of medical device requirements, change notices, and dFMEA required. 2.Familiarity with task management sy