Quality Engineer

The Successful ApplicantBachelor's degree in Engineering3+ years of experience in manufacturing/quality2 years of work experience with regulated electro-mechanical medical products in a manufacturing environmentAbility to manage multiple, simultaneous projects and deadlinesAbility to synthesize and document requirementsExcellent written and verbal communication skillsMust be able to work independently, in a team environment, and with cross-functional teamsWorking knowledge of Statistical software package Minitab, InfinityQS, Microsoft Word and ExcelExperience in internal auditing of Quality Management SystemsSPONSORSHIP NOT PROVIDEDWhat's on OfferCompensation up to $95,000 (DOE)3 weeks of PTOMedical, dental, and visionShort term/long term disabilityTuition reimbursementJob SummarySector: Engineering & ManufacturingSub Sector: Quality, TechnicalIndustry: Industrial / ManufacturingLocation: CarpentersvilleContract Type: PermanentConsultant name: Max SintonJob Reference: JN-072026-7058518 Their solutions support specialties such as urology, gastroenterology, laparoscopy, and endoscopy, helping improve patient outcomes, surgical efficiency, and safety; they are seeking a skilled Quality Assurance Engineer to join the team.

Quality Assurance EngineerOur client has been a leader for 40+ years in developing and manufacturing innovative medical devices for minimally invasive surgical procedures. Their solutions support specialties such as urology, gastroenterology, laparoscopy, and endoscopy, helping improve patient outcomes, surgical efficiency, and safety; they are seeking a skilled Quality Assurance Engineer to join the team.Job DescriptionEstablish activities for the development, application and maintenance of quality standards for processes, finished devices, materials, and other productsDevelop standards and methods for inspection, testing, and evaluation, utilizing knowledge in engineering fields such electrical, and mechanicalDevelop sampling procedures, forms and instructions for recording, evaluating, and reporting quality and reliability dataDevelop methods and procedures for disposition of discrepant material and devise methods to assess cost and responsibilityCollaborate with Regulatory affairs to meet the requirements of the FDA and Medical Device DirectiveManage CAPA program for areas of responsibilityMPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.The Successful ApplicantBachelor's degree in Engineering3+ years of experience in manufacturing/quality2 years of work experience with regulated electro-mechanical medical products in a manufacturing environmentAbility to manage multiple, simultaneous projects and deadlinesAbility to synthesize and document requirementsExcellent written and verbal communication skillsMust be able to work independently, in a team environment, and with cross-functional teamsWorking knowledge of Statistical software package Minitab, InfinityQS, Microsoft Word and ExcelExperience in internal auditing of Quality Management SystemsSPONSORSHIP NOT PROVIDEDWhat's on OfferCompensation up to $95,000 (DOE)3 weeks of PTOMedical, dental, and visionShort term/long term disabilityTuition reimbursementJob SummarySector: Engineering & ManufacturingSub Sector: Quality, TechnicalIndustry: Industrial / ManufacturingLocation: CarpentersvilleContract Type: PermanentConsultant name: Max SintonJob Reference: JN-072026-7058518