Assistant Manager-Analytical Reviewer & IPQA

The candidate must have hands-on experience and working knowledge of:

• Potentiometer Metrohm
• GC (Gas Chromatography)
• Polarimeter
• TOC Analyzer
• Dissolution Test Apparatus
• Microbiological testing / basic Microbiology knowledge
• QC Documentation and Analytical Data Review
• Review of analytical reports, test results and related QC documentation

The candidate should have practical experience in:

• IPQA activities for Tablets, External Liquids and Topical Preparations
• In-process and finished-product quality checks
• Batch documentation review
• Batch Release activities
• Process Validation
• Line clearance and in-process compliance
• GMP/GDP compliance and documentation practices

Preferred candidate profile

• Strong understanding of GMP, GDP, QC and IPQA requirements.
• Good analytical review and documentation skills.
• Ability to independently handle QC/IPQA responsibilities.
• Strong attention to detail and compliance-oriented approach.
• Candidates should have relevant pharmaceutical manufacturing experience.
• 5 or 6 years of experience in QC Laboratory / Analytical Operations.
• 2 or 4 years of experience in IPQA.
• Experience in Tablets, External Liquids, and Topical Preparations is required.