About AJR Enterprises:

AJR Enterprises, a UFP Technologies company, is a leader in developing and manufacturing single use safe patient handling systems; specializing in 'cut and sew' manufacturing services and advanced fabric technologies.

UFP Technologies, Inc. offers a competitive benefits package, including but not limited to:

Medical, Dental, Vision, Life, Disability Insurance401K with a matching contributionPaid time off, Paid holidays, Employee discounts and much more!

Location:

This position will be on-site full-time in St. Charles, IL. The position holder will need to be within commuting distance (within 45 min).Applicants must be authorized to work for any employer in the U.S. At this time, we are unable to sponsor or assume sponsorship of an employment visa.

Quality Engineer Summary:

This position ensures that the quality related engineering needs of the organization are met. Responsibilities include compliance and risk analysis, process validation, pFEMAs, IQ, OQ, PQ and PPQ validation, CAPA and etc. Position works in collaboration with operations, supply chain, new product development teams.

Quality Engineer Duties and Responsibilities:

Lead in supporting compliance for medical device manufacturer in ID/Traceability throughout supply chain, well documented and executed Acceptance Activities, Non-conforming material management, Packaging/Labeling control, Production/Process controls, Process Validation.

Risk Assessments, project meetings, pilot builds, First Article Inspections, and Post Market Risk ManagementDesigns and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and/or production equipment Design and execution of pFEMAs, IQ, OQ, PQ and PPQ validation Corrective and Preventive Action management, facilitation, ownership and problem resolutionProcess improvement and support, including Quality System process review and revisionTraining assistance, including providing training in quality system activities/requirementsInternal and external audit coordination and facilitationPerforms all other duties as needed.

Quality Engineer Qualification Requirements:

A Bachelor's degree in science, engineering or equivalent3-7 years relevant experienceAt least 3 years experience in medical device manufacturingStrong knowledge of Quality Systems policies and regulations (ISO 13485 and FDA Part 820) with a strong background in medical device quality assurance and processesExperience conducting supplier audits and writing supplier contractsFamiliarity with statistical analysisUFP Technologies, Inc. is an Equal Opportunity/Affirmative Action employer Minorities/Women/Veterans/Disabled.#UFP #IL #IND