Quality Engineer jobs in Dexter

Katalyst Healthcares & Life Sciences

Job Summary: Quality Engineer II with experience in medical device manufacturing, process validation, and quality systems compliance within FDA-regulated and EU MDR environments. Skilled in IQ/OQ/PQ validation, process characterization, PFMEA, control plans, risk management, SOP development, and cha

Job Description: We are looking for an experienced Supplier Quality Engineer with 6–8 years of experience in supply chain, operations, engineering, or quality management within regulated industries such as Medical Devices, Pharmaceuticals, or Life Sciences. The candidate should have experience manag

Job Description: Quality Engineer supporting MDR remediation and manufacturing quality for medical device products, focusing on process validation, risk management, and change control. Responsibilities : Execute process & test method validations (IQ/OQ/PQ). Perform First Article Inspections (FAI

Join our team in Dexter, MI, a vibrant community that offers a perfect blend of small-town charm and modern amenities. Enjoy a fulfilling career in a location known for its beautiful parks, excellent schools, and a strong sense of community. Must Have Experience in equipment IQ Experience in OQ (Ope

Job Description: We are seeking an Quality Complaint Investigation to support complaint investigations, quality system activities, and continuous improvement initiatives within a regulated medical device manufacturing environment. The role involves analyzing quality data, conducting root cause inves

Job Summary: Quality Engineer II with experience in medical device manufacturing, process validation, and quality systems compliance within FDA-regulated and EU MDR environments. Skilled in IQ/OQ/PQ validation, process characterization, PFMEA, control plans, risk management, SOP development, and cha

Job Description: We are seeking an Quality Complaint Investigation to support complaint investigations, quality system activities, and continuous improvement initiatives within a regulated medical device manufacturing environment. The role involves analyzing quality data, conducting root cause inves