Manufacturing Engineer
Job
Kelly Services Inc.
Brooksville, FL (In Person)
$135,000 Salary, Full-Time
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Job Description
Manufacturing Engineer Apply Now Applied To save a job sign in or get started
Job ID:
10164070 Posted today Back Brooksville, FL, US Engineering Bachelors Degree Full Time, Direct Hire 120,000- $150,000 Experienced (Non-Manager) On-site Engineering Services First Shift (Day) Brooksville, FL, US 120,000
- $150,000 Experienced (Non-Manager) Full Time, Direct Hire Engineering Services On-site Engineering Bachelors Degree First Shift (Day) Apply Now Applied Job details
Job Title:
Manufacturing Engineer Location:
Brooksville, FL (Relocation assistance available)Job Type:
Direct Hire Salary:
$120,000- $150,000
Work Authorization:
Must be able to work in the U.S. without sponsorship Position Overview We are seeking a proactive and detail-oriented Manufacturing Engineer to serve as a key link between Engineering and Production within our ISO 13485-compliant medical device manufacturing environment. This role is responsible for developing, validating, and sustaining robust manufacturing processes, as well as maintaining accurate documentation and leveraging quality systems to ensure product reliability, regulatory compliance, and operational efficiency. Key Responsibilities Process Development & Documentation Develop, implement, and maintain manufacturing routers, work instructions, and Standard Operating Procedures (SOPs). Create and update process flow diagrams and Process Failure Mode and Effects Analyses (PFMEAs). Lead and support process validation activities (IQ/OQ/PQ) in compliance with ISO 13485 and FDA requirements. Conduct First Article Inspections (FAI) and ensure complete documentation and traceability. Collaborate with Quality to develop and maintain Production Part Approval Process (PPAP) documentation. Evaluate existing tools and fixtures for effectiveness; design and develop new tooling and fixtures using CAD software (e.g., SolidWorks) as needed. Design and implement incoming inspection processes for raw materials and components. Monitor nonconforming materials, lead root cause investigations, and define appropriate rework or corrective actions. Support and actively participate in Corrective and Preventive Action (CAPA) processes. Conduct and analyze Statistical Process Control (SPC) studies to monitor, control, and improve process performance. Training & Production Support Train production personnel on new and revised manufacturing processes, procedures, and equipment. Provide hands-on technical support to resolve production issues and improve process capability and efficiency. Continuous Improvement Partner with cross-functional teams to identify, prioritize, and implement process improvements. Drive initiatives to reduce waste, improve efficiency, and enhance overall manufacturing performance. Required Qualifications Bachelor's degree in Mechanical, Manufacturing, Biomedical Engineering, or a related field. 3-5 years of experience in a regulated manufacturing environment, preferably within the medical device industry. Strong working knowledge of ISO 13485 and FDA regulatory requirements. Hands-on experience with process validation (IQ/OQ/PQ), FAI, PFMEA, SPC, and PPAP documentation. Proficiency with CAD software, ERP systems, and Microsoft Office Suite. Excellent technical documentation, communication, and organizational skills. 10164070 Share this job Copied url To save a job sign in or get started To apply for this job email your details to I want more jobs like this in my inbox.GET JOB ALERTS
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- $150,000 As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources.
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