Documentation, HPLC, OOS/OOT, Documents Review - AQA

We are looking for an AQA professional to manage documentation, perform and review HPLC analysis, and handle OOS/OOT investigations. The role involves reviewing quality documents, ensuring GMP compliance, supporting audits, and maintaining data integrity. The ideal candidate should have strong knowledge of analytical quality assurance, regulatory guidelines, and excellent attention to detail.

Overview

• Industry - PHARMACEUTICAL / MEDICAL DEVICES / CRO
• Job Role - Other
• Employment type - Full Time - Permanent
• Work Mode - In Office

Qualifications

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

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