Job Description :
Manufacturing engineer with Medical device exp
Location: North Haven,CT
12 month
Full time contract both are open

CONDUCT, COORDINATE AND AID IN EQUIPMENT VALIDATION (IQ) & PROCESS VALIDATIONS (OQ/PQ) INCLUDING PROTOCOL
ENSURE NEW PROCESSES HAVE ADEQUATELY DEMONSTRATED SPECIFIED PROCESS AND TEST CONTROL CAPABILITIES, THROUGH BEING THE CHAMPION FOR PFMEA, DFM, DFT, DFSS, CAPA AND NCR
PROVIDE GUIDANCE IN DESIGNS AND EVALUATES NEW AND EXISTING FIXTURES AND EQUIPMENT, TEST METHODS, SPECIFICATIONS, LAYOUTS, AND STANDARDS SUPPORTING A LEAN MANUFACTURING ENVIRONMENT
MANAGE TECHNICAL ASPECTS OF PRODUCT AND PROCESS TRANSITION TO CONTRACT MANUFACTURING PARTNERS
ENSURE MANUFACTURING PROCESSES ADEQUATELY DEMONSTRATE SPECIFIED PROCESS CONTROL CAPABILITIES
MANAGE ALL TECHNICAL ASPECTS OF THE ECO PROCESS (AGILE)
PROVIDE TECHNICAL SUPPORT AND GUIDANCE TO CONTRACT MANUFACTURER FOR ENGINEERING ISSUES
MANAGE LOCALIZATION ACTIVITIES WITH CONTRACT MANUFACTURING AND SUSTAINING ENGINEERING
SPECIFY AND PROCURE CAPITAL IN THE SUPPORT OF MANUFACTURING AND TEST PROCESSES
ABILITY TO WORK INDEPENDENTLY AND BE ABLE TO COMMUNICATE EFFECTIVELY WITH SUPERIORS, SUBORDINATES, AND CONTRACTORS
SELF-DIRECTED WITH THE ABILITY TO DEVELOP, FACILITATE AND GAIN CONSENSUS IN A TEAM ENVIRONMENT
ABILITY TO ADAPT TO EVOLVING PROJECTS REQUIREMENTS