Under general supervision, plan and execute verification and validation activities to ensure regulatory compliance. Inspect, measure, analyze, audit, calibrate, and test instrumentation, equipment, software and hardware, machines, and procedures. Identify problems and their sources, correct them efficiently, implement process improvements, and identify product improvement opportunities. Create and document an evidence trail demonstrating that testing procedures and protocols are accurate and meet regulatory requirements. Test and evaluate products of moderate to advanced complexity, interpret data, and assess performance against product requirements and design inputs. Execute and help develop verification and validation protocols, and prepare reports for regulatory audits, submissions, and requests. Maintain thorough documentation throughout the verification and validation lifecycle. Analyze test results and contribute to design and failure investigations, root-cause analysis, risk assessment, and evaluation of regulatory compliance. Assist with test-method development, including fixture design, equipment acquisition, and hardware/software validation. Work with design and development teams to establish product requirements based on user needs, regulatory strategy, and applicable standards. Manage assigned projects, timelines, and goals. Medline Industries, LP, offers a competitive total rewards package, continuing education and training, and potential for growth in a worldwide organization. This position is bonus and/or incentive eligible. Benefits vary based on average hours worked per week. The company describes its commitment to inclusion, belonging, and equal opportunity.
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Job Type
Full-time
Career Level
Mid Level