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Job Function:
Supply Chain EngineeringJob Sub Function:
Quality EngineeringJob Category:
Scientific/TechnologyAll Job Posting Locations:
Plymouth Minnesota United States of AmericaJob Description:
Employer: SterilMed Inc
Job Title: Senior Quality Engineer
Job Code: A011.7755
Job Location: Plymouth MN
Job Type: Full-Time
Job Duties: Develop measurement systems to monitor the effectiveness of QA and reliability systems to identify bracket correct and prevent defects demonstrating continuous improvement to management. Provide support and expertise in the implementation and enforcement of GMP ISO and FDA requirements and maintain alertness to changes in the industry and regulatory environments applying this information to business practices. Prepare QA systems and assist in technical issues for manufacturing processes that are to be transferred to satellite facilities. Manage established processes in support of steady-state manufacturing in accordance with the defined QA program for product transfers. Provide statistical support and expertise in DOE (Design of Experiments) and analytical problem solving for manufacturing technical services and product development to minimize sample and scrap waste assess reliability and risks based on data presented identify root causes of problems and reduce and identify sources of variation. Audit and approve manufacturing quality engineering and validation/qualification documents for conformance to company business practices and departmental procedures. Support the development of validation strategies and act as a liaison to the Regulatory Affairs department to perform initial regulatory reviews of all engineering changes/modifications to products. Perform analysis of documents and information to ensure that all critical product characteristics have been identified and properly evaluated including design specifications FMEA (Failure Mode Evaluation and Analysis) for product and process material specifications QA system (in-line control points) - FGI results product inquiry analysis reliability analysis and R&D Laboratory support. Provide sampling plans and approve inspection methods for evaluation and testing of components and products. Support the Continuous Release program where applicable to reduce the need for FGI inspection and provide support and expertise in reliability strategy and reliability growth demonstration during new product development.
Requirements: Employer will accept a Masters degree in Biomedical Engineering Systems Engineering Quality Engineering Management Business Management or related field and three years of experience in job offered or in a Senior Quality Engineer -related occupation.
This job posting is anticipated to close on 8/11/2025.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
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Required Experience:
Senior IC
Full-Time