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DescripciónDescription
Sr. Engineer with working knowledge and experience with engineering practices and cGMP procedures on pharmaceutical/biotech production process, facilities, and equipment.
Knowledge and experience in:
Technical Writing
Quality Risk Assessments such as FMEA and/or QRAES
Change Control
Non-Conformance
Corrective and Preventive Maintenance
Validation Practices
Escorting Vendors
Shift: 8hrs - 1st shift | 8AM-5PM
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Requisitos Requirements
Doctorate 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)(Oral/Write)
Technical Writing
Validation Processes knowledge
Work schedule flexibility as required to support 24/7 operations, requiring occasional after-hours engineering coverage.?
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AVISO de ClasificadosOnline
Los patronos NO le piden dinero ni un depósito para trabajar, si lo piden es un negocio, inversión o Fraude.
NO envíe dinero para trabajar, tampoco ofrezca información personal, por teléfono o email. Evite el Fraude
ClasificadosOnline Warning
Employers DON'T ask for money or deposits for work, if they do is a bussiness, invertion or Fraud.
DON'T send money for work, neither offer personal information, by phone or email. Avoid the Fraud
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Empleos en Puerto RicoJobs in Puerto Rico
QRC GROUP LLC
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