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.
Requirements
Doctorate or Masters + 2 years of Engineering experience or
Bachelors in Engineering + 4 years of Engineering experience.
Excellent written and verbal communication skills
Technical writing experience
Independent, self-motivated, organized, able to multi-task in project environments, and skilled in communication, facilitation, and collaboration
