Job Title : Senior Quality Engineer
Job Location : Sturtevant, WI
Job Type : 5+ Months contract
This position is responsible for providing Quality Engineering and Technical Support for Operations, Sustaining Engineering, R&D, and New Product Introductions. This position would include supporting a wide array of activities related to Change Control, NCR / CAPA, Quality Operations, Design Control, New Product Development, Risk Management and Post Market Surveillance. This position would evaluate the operation of Manufacturing and Quality activities in relation to compliance to Quality Standards and Regulations and recommend where corrections or improvements are needed. Provide direct support to Quality personnel regarding operation of the department and Quality System. Provide support to other departmental activities as directed.
Job Responsibilities :
Change Control :
- Review change requests and identify impact on product design and documentation
- Support Change Control Activities (Operations, Engineering, Design, etc.)
- Support updates to manufacturing procedures, process, product / specifications, risk management files, etc. through the Change Control process
- Support 3rd party supplier management activities such as review 3rd party design control activities
Design Control / Documentation :
Review documentation for technical accuracy and compliance to proceduresReview Technical Writing and DocumentationSupport operations, sustaining engineer, R&D and NPI departments in the development, verification and validation of product changes and introduction of new productsQuality initiatives :
Provide quality engineering support for supplier changes and resolution of issues at suppliersIdentifies new quality improvement initiatives / projects in accordance with cGMP expectations to improve compliance, quality levels (reducing defects), and improve operational efficienciesWorks with manufacturing and other functional groups on manufacturing regulatory compliance issueSupport training program by delivering assigned training tasksSupport NCR and CAPA :
Support / lead corrective / preventive actions and product non-conformances including capturing data and investigations associated with product deviations, product non-conformances, CAPAs, scrap and rework, and analyzing the data for the reasons of Quality Improvement and reportingRisk Management :
Support Risk Management activities including review and coordination of quality activities related to riskInspections :
Support with federal, state, and local regulatory officials during regulatory inspections Support in internal and vendor quality system audits as applicableAdherence to regulations :
Assist with adherence to all Federal, State and Local Regulations controlling the manufacture of Electromechanical Devices (EMD) and non-EMD medical devicesSkills & Experience Required :
Bachelor of Science (B.S.) Physical Science or Engineering3-5 years Quality Engineering role6-7 years Medical Device or Pharmaceutical IndustryASQ Certification as a Quality Engineer preferredFamiliar with ISO 13485 Quality System Standards, FDA Quality System Regulations, GMPs, and / or other international medical device regulations