Sr Engineer with knowledge and experience with cGMP procedures and engineering practices on pharmaceutical/biotech production processes, facilities, and equipment. Experience with QRAES, Change cControl, non conformance, corrective and preventative actions, and validation practices. Experience with Maximo Capable of working and/or submitting Purchase Orders (PO). Experience working and escorting vendors. Capable of handling multiple tasks, projects and/or priorities at the same time. Work schedule flexibility as required to support 24/7 operations, requiring occasional after-hours engineering coverage.
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Job Type
Full-time
Career Level
Senior
Number of Employees
1-10 employees