Quality Eng - P2
Core
Develops and maintains quality engineering methodologies, systems, and practices to meet regulatory and customer requirements for product development, qualification, and manufacturing.
Role type
Quality Engineer
Builds
Process control systems, validation protocols, test documentation, and streamlined business systems for product quality.
Domain
Medical device manufacturing and regulatory compliance
Required skills
project management, validation, problem solving, people management
Preferred skills
medical device background, project transfer experience
Technologies
validation techniques, regulatory compliance frameworks
Responsibilities
Identify and implement process control systems for product development and manufacturing; Create and revise departmental procedures; Apply systematic problem-solving methodologies to resolve quality issues; Develop testing and inspection methodologies and documentation; Review and develop validation protocols and reports; Interface with engineering departments, customers, and suppliers on quality issues.
Seniority
Mid-level, hands-on IC