- 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 change control, 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.
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Sr Engineer - 35077 - Juncos, PR - Integrated Services For Productivity & Validation, Inc
Descripción
Bachelor's Degree in Engineering, preferred Mechanical, Electrical, or ChemicalRequirements
Doctorate OR Masters + 2 years of Engineering experience ORBachelors in Engineering + 4 years of Engineering experience
Shift: 8hrs (first)
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