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Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions. Apply now for the position of Automation Engineer, where you will be responsible for the successful design, implementation, validation, and support of custom automated systems reporting to the Director of Engineering. This role will be part of a team of engineers that will support manufacturing and drive functional excellence across the Walpole Site. Your role includes identifying and implementing manufacturing processes and/or equipment productivity improvements related to controls and automation. You will develop and execute manufacturing processes, equipment, and testing validation strategies, documenting as required (IQ, PQ). Monitoring the manufacturing SQL databases and equipment performance, supporting patches, tests, and evaluations, and documenting as required will also be part of your responsibilities. You will prepare manufacturing equipment User Requirement Specifications (URS) and collaborate cross-functionally while working on multiple projects simultaneously. Your expertise should include strong PC skills and familiarity with common PLC and .NET framework applications, with experience in a manufacturing environment. You should have the ability to integrate and execute change control for process and hardware solutions, and experience working with Siemens Opscenter Manufacturing Execution System (MES). Excellent knowledge of database design, documentation, and SQL coding is required, along with strong broad-based automation and electro-mechanical design experience and industrial controls system knowledge. An understanding of industrial networking and Virtual Machines within a manufacturing environment is also necessary. Strong communication, presentation, and documentation skills in a team environment are essential. Experience working in an FDA, ISO9000, GMP, or another regulated environment is required, and experience in Medical Device manufacturing is desired.
