Job Description
Sr Engineer with knowledge and experience with: cGMP procedures and engineering practices on pharmaceutical/biotech production processes, facilities, and equipment. Change control, non-conformace, corrective and preventive actions, and validation practices. Maximo. Working and/or submitting Purchase Orders (PO). Working and escorting vendors. Requirements Doctorate or Master's Degree +2 years of engineering experience or Bachelor in Engineering +4 years of engineering experience (Mehcanic, Electrical or Chemical) Technical Writing Bilingual (Spanish/English)(Write/Speak) Work schedule flexibility as required to support 24/7 operations, requiring occasional after-hours engineering coverage.
4 years
4 years