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Validation Specialist (QC Equipment with CSV )

Yauco, PR · Biotech/Pharmaceutical
Responsibilities:
•    Validation Specialist for QC Equipment with CSV knowledge   (FTIR-Spectrophotometer for ID and Nebula-Endotoxins Equipment)

Qualifications:
    • Experience in Lab Equipment with computer systems
    • 3-5 years of experience
    • Validation experience
    • Generation of protocols
    • Review and approval of documents
    • Use of electronic system to manage documents
    • Background on QC Lab Requirements for qualification
    • Could be a Microbiologist, Chemist, or Engineer


**Weil Group is proud to be an Equal Employment Opportunity Employer.*

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