Lead Associate - Quality Assurance (Manufacturing)

• Responsible for supporting management of the Quality System with a focus on continuous improvement and responsibility for ensuring compliance with cGMP, FDA requirements, and internal SOPs.
• Manage Reserve sample programs while adhering to internal procedures.
• Manage process for review of artwork and specification changes for labelling.

Overview

• Industry - PHARMACEUTICAL / MEDICAL DEVICES / CRO
• Functional Area - IT Software Programming / Analysis / Quality / Testing / Training
• Job Role - Software Quality Assurance Analyst
• Employment type - Full Time
• Work Mode - In Office

Qualifications

• Any Graduate - Any Specialization
• Any Post Graduate - Any Specialization
• Any Doctorate - Any Specialization

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