Jt883 - Manufacturing Engineer II

• Execute equipment & test method validations, perform manufacturing procedure changes.
• Reviews the work of other specialists; may manage some elements of  projects. 
• Conduct Test Method Validation Analysis
• Change control of Medical Devices
• Equipment Commissioning / Qualification
• Process Validation
• Computer System Validation (CSV)
• Manufacturing, Packaging and Laboratory Equipment
• Technical experience (Trouble shooting) or any similar experience or background
• Quality / Process Control / Assurance of Medical Device
• Perform documentation changes processes. 
• Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality. 
• Ensures processes and procedures are in compliance with regulations.
• Contributes to the completion of work group objectives, through building relationships and consensus to reach agreements on assignments.

• Bachelor’s degree in engineering (Electrical, Mechanical, Industrial preferred).
• 2+ years of Engineering experience in Medical Device industry
• Computer system & Equipment (non-CSV), test method validations
• Documentation changes
• Availability to work extended hours including weekends, great team work
• Process Validation and Computer software validation knowledge.
• Equipment Validations Manage Supplier Change Requests
• 1st shift

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.