• 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
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