Manufacturing Engineer

Manufacturing Engineer Apply Now Applied To save a job sign in or get started

Job ID:

10229201 Posted today Back Memphis, TN, US Engineering Bachelors Degree Full Time, Temporary $30

• $34 per hour based on experience Experienced (Non-Manager) On-site Medical Devices and Supplies First Shift (Day) Memphis, TN, US $30
• $34 per hour based on experience Experienced (Non-Manager) Full Time, Temporary Medical Devices and Supplies On-site Engineering Bachelors Degree First Shift (Day) Apply Now Applied Job details

Job Title:

Manufacturing Engineer Location :

Memphis, TN•

Onsite Duration:

17+ months with possible extensions

Pay:

$30

• $34 per hour based on experience

Position Summary:

As a contract Engineer, you will contribute to cleaning and passivation systems under the supervision of a cleaning SME for orthopedic medical devices. You will execute validation activities, support engineering testing, and drive project plans within a regulated manufacturing environment. In this role, you will develop technical depth in learning and validation while supporting larger projects and cross-functional initiatives. Responsibilities

• Help draft, review, execute, and document Cleaning Validation Protocols (IQ, OQ, PQ)
• Support the installation, startup, and verification of new cleaning equipment
• Use precision measuring tools to verify equipment layouts against blueprints and confirm fit within physical spaces and utility configurations
• Troubleshoot cleaning equipment to optimize cleaning programs and process parameters required for medical implants
• Investigate and resolve cleaning deviations or out-of-specification (OOS) results
• Conduct risk assessments to prevent cross-contamination between medical device products
• Execute cleaning trials and process studies to optimize parameters such as time, temperature, and detergent concentration prior to formal validation
• Perform fixture testing to ensure complex devices are properly held, cleaned, rinsed, and dried during automated cleaning cycles
• Perform root-cause analysis to investigate cleaning failures or process deviations
• Create, revise, and maintain Standard Operating Procedures (SOPs) and Work Instructions to reflect validated cleaning processes
• Directly train or support the training of production personnel on updated cleaning processes and procedures
• Work cross-functionally with Manufacturing Engineering, Quality, Validation, and Operations teams
• Perform other duties as assigned by the Project Manager or Senior Engineer. Required Education
• Bachelor of Science in Engineering required
• Master of Science in Engineering desired Experience
• 2-4 years of manufacturing engineering experience in a regulated industry; medical device preferred.
• Basic experience using AutoCAD or DraftSight to update and maintain existing floor plans and equipment layouts
• Familiarity with validation activities (URS, FDS, IQ, OQ, PQ, VRA) is required.
• Knowledge of cleaning and passivation preferred Physical Demands
• Standing and walking in production areas for extended periods.
• Lifting objects up to 40 lbs. occasionally.
• Use of personal protective equipment (PPE) as required.

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