4 months QC Specialist (Equipment Qualification, Protocol Writing, Pharmaceutical MNC) #HCG

About this role

Responsibilities Perform equipment qualification activities, including preparation and execution of qualification protocols and reports. Develop, review, and maintain equipment qualification documents in compliance with cGMP and applicable quality standards. Support QC release activities, including

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• Healthcare / Pharmaceutical
• Sciences / Laboratory / R&D
• FTIR
• Standard Operating Procedures
• Good Documentation Practices
• Sampling

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