*Date Posted: *01/18/2024

　　*Hiring Organization: *Rose International

　　*Position Number: *456908

　　*Job Title: *Product Acceptance Engineer

　　*Job Location: *Kalamazoo, MI, USA, 49001

　　*Employment Type: *Temporary

　　*Estimated Duration (In months): *18

　　*Min Hourly Rate($): *40.00

　　*Max Hourly Rate($): *47.00

　　*Must Have Skills/Attributes: *Analysis, Design, Testing

　　Only those lawfully authorized to work in the designated country associated with the position will be considered.

　　Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client's business needs and requirements.

　　Product Acceptance EngineerLocation: Kalamazoo, MI 49002Duration: 18 months -- potential longer term extension or conversion

　　CONSULTANT MUST WORK ONSITEOur client is an American multinational medical technologies corporation based in Kalamazoo, Michigan and has 29 office locations located throughout the US. They offer innovative products and services in Medical and Surgical, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes.

　　The client's products include implants used in joint replacement and trauma surgeries; surgical equipment and surgical navigation systems; endoscopic and communications systems; patient handling and emergency medical equipment; neurosurgical, neurovascular and spinal devices; as well as other medical device products used in a variety of medical specialties.

　　The Product Acceptance Engineer will be the primary contact between Quality Assurance and Operations in The Finished Goods Operations. This person will provide expert QA and scientific support to Operations, in ensuring goals and objectives are achieved for The Finished Goods Operations. The engineer will be applying product release process, for new projects coming into FGO

　　Duties:• Complete Lot Review and Release for The Finished Goods Operations.• Complete Sterile load reviews• Continuous improvement and development of acceptance and inspection activities in The Finished Goods Operations.• Introduction of best practices in acceptance and inspection activities.• Co-ordinate with business units to ensure that acceptance and inspection activities are appropriately carried out.• Ensure that a consistent approach to acceptance and inspection activities is developed and maintained.• Co-ordinate with the business units in relation to non-conformance activities and root cause analysis associated with acceptance and inspection activities, to ensure a consistent approach.• Provide effective and responsive QA support to Operations to resolve in-house, customer and supplier issues.• Ensure regulatory compliance in area of responsibility to GMP of all medical device's regulatory agencies (i.e. FDA, IMB and BSI).• Provide functional expertise to other support function on quality related issues.• Own and drive NC/CAPA's related to pr