Quality Assurance Engineer

Integrated Resources, Inc

Madison, Wisconsin

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JOB DETAILS

JOB TYPE

Contractor

SKILLS

Change Control, Clinical Research, Code of Federal Regulations, Design Document, Distribution Services, FDA (Food and Drug Administration), ISO (International Organization for Standardization), Information Technology & Information Systems, Maintain Compliance, Manufacturing, Manufacturing Methods, Manufacturing/Industrial Processes, Medical Equipment, Process Control Engineering, Process Flow Diagram (PFD), Process Validation, Product Development, Product Lifecycle, Product Planning, Production Control, Quality Assurance, Quality Assurance Methodology, Regulatory Requirements, Rehabilitation Nursing, Validation Plan, Validation Testing, Verification Plans

LOCATION

Madison, Wisconsin

POSTED

1 day ago

Quality Assurance EngineerIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job Description· The Quality Leader is responsible for providing manufacturing support in accordance with documented procedures and practices.· This is a key technical role responsible for the development, implementation, improvement and continuous reinforcement of established QA fundamental practices that are utilized in the local business.· The role involves hands-on work in the areas of design, design transfer, manufacturing, distribution, and service.· Ensures process efficiency and compliance effectiveness through the development and implementation of process verification and validation plans, including Master Validation Plans (Site Level), Validation Master Plans (Product or Process specific plans), and the development of simple yet detailed process flow diagrams that describe critical process interdependencies with respect to process inputs, outputs, risks and impacts.Qualifications· Bachelor's Degree in an engineering or technical discipline (or non-technical degree with 2 years of experience in manufacturing, engineering or quality assurance experience in addition to any other experience requirements).· Demonstrated understanding or aptitude to understand Medical Device QMS requirements and regulatory requirements including but not limited to FDA CFR 21 820 and ISO 13485.· Demonstrated understanding of product development lifecycles, design change and document change control, process verification and validation methodologies, manufacturing / production process control methodologies, and servicing in a medical device environment.

Quality Assurance Engineer

Integrated Resources, Inc

Madison, Wisconsin

About the Company

Integrated Resources, Inc

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