Save Job Back to Search Job Description Summary Similar JobsOwn process development, validation, and manufacturing documentation.Improve production efficiency while maintaining regulatory compliance.About Our ClientOur client is a growing medical device manufacturer focused on delivering high-quality products through a strong commitment to quality, regulatory compliance, and continuous improvement. The organization offers a collaborative environment where engineering professionals can make a direct impact on manufacturing performance and product quality.Job DescriptionIdeal Candidate:Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Biomedical Engineering, or a related technical discipline.3-5+ years of experience in a regulated manufacturing environment, preferably within medical devices.Strong understanding of ISO 13485 requirements and quality systems.Experience with process validation, PFMEA, FAI, SPC, CAPA, and PPAP documentation.Proficiency with CAD software, ERP systems, and Microsoft Office applications.Familiarity with risk management methodologies and statistical analysis tools such as Minitab.Excellent communication, documentation, and organizational skills.Proven ability to work effectively across Engineering, Quality, and Production teams.MPI 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 ApplicantA successful 'Manufacturing Engineer' should have:Experience with manufacturing engineering activities and process improvement.Ability to assess production issues and develop practical solutions.Experience creating and maintaining manufacturing documentation.Knowledge of production methods, tools, and equipment.Ability to review process results and identify improvement opportunities.Experience working with engineering and manufacturing teams.What's on OfferWhat's To Offer:Opportunity to join a growing medical device manufacturer with a strong quality-focused culture.Exposure to process development, validation, and continuous improvement initiatives.Collaborative cross-functional work environment.Competitive compensation and benefits package.Career growth opportunities within engineering and operations.ContactJosephine BelcherQuote job refJN-112026-7143820Job summarySectorEngineering & ManufacturingSub SectorEngineering Design and R&DIndustryIndustrial / ManufacturingWhereSpring HillContract TypePermanentConsultant nameJosephine BelcherJob ReferenceJN-112026-7143820