Our client is a growing medical device manufacturer in the Raleigh area looking for a Quality Engineer to join their team on a contract basis. This role sits at the center of production and quality, giving someone the chance to make a real impact on product compliance, process improvement, and day-to-day manufacturing quality in a regulated manufacturing environment. Quality Engineer Responsibilities: -Lead and support quality issue management, including investigation, containment, and resolution of complaints and nonconformances - Drive root cause analysis and corrective action activities, ensuring proper disposition and documentation - Support new product introductions and product transfers, ensuring manufacturing readiness and compliance with quality requirements - Partner with Operations and Engineering on continuous improvement projects, process validations, and manufacturing quality initiatives - Analyze and report on quality metrics and trends to support production and quality planning Quality Engineer Requirements: - 2 to 5 years of experience in Quality Engineering or Manufacturing Quality within a regulated industry, medical device experience strongly preferred - Knowledge of quality system principles, along with experience in nonconformance reporting, complaint handling, and CAPA processes - Familiarity with new product introduction and product transfer processes; strong problem-solving and root cause analysis skills - Strong verbal and written communication skills, with the ability to interpret technical drawings and regulatory documents - Bachelor's degree in Engineering (Mechanical, Industrial, Biomedical, or related field) preferred
Not specified in the original listing.
Not specified in the original listing.
Synerfac Technical Staffing is a leading service provider in the staffing sector, focusing on finding skilled professionals to join companies in various technical fields. The company emphasizes collaboration, integrity, and effective communication wi... Read More