Descripcion
Sr Engineer with working knowledge and experience with cGMP procedures and engineering practices on pharmaceutical/biotech production processes, facilities, and equipment. Experience with change control, non conformance, corrective and preventative actions, and validation practices. Experience with Maximo. Capable of working and/or submitting Purchase Orders (PO).
Work schedule flexibility as required to support 24/7 operations, requiring occasional after-hours engineering coverage.
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Requisitos - Requirements
Doctorate degree or Master’s degree and 3 years of Engineering experience or
Bachelor’s degree in Engineering and 5 years of Engineering experience
Bilingual (Spanish/English)
Technical writing
Capable to handling multiple tasks, projects and/or priorities at the same time.
Experience working and escorting vendors.
Work schedule flexibility as required to support 24/7 operations, requiring occasional after-hours engineering coverage.
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