Excellent written and verbal communication skills Technical writing experience Working 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 Independent, self-motivated, organized, able to multi-task in project environments, and skilled in communication, facilitation, and collaboration Work schedule flexibility as required to support 24/7 operations, requiring occasional after-hours engineering coverage. Requirements -Doctorate OR Masters + 2 years of Engineering experience OR -Bachelors in Engineering + 4 years of Engineering experience. 8 hrs shift (1st)
-Doctorat...