Assistant Manager-Analytical Reviewer & IPQA

G.S. Pharmbutor Private Limited (Betadine Plant); Ghaziabad District; On-site; INR 600,000 - 900,000; Full time

Job summary

G.S. Pharmbutor Private Limited (Betadine Plant) is seeking a QC/IPQA professional with hands-on experience in analytical operations and batch documentation review.

The role focuses on IPQA activities for tablets, external liquids, and topical preparations, along with in-process and finished-product QC checks. The ideal candidate will have 5–6 years in QC Laboratory / Analytical Operations and 2–4 years in IPQA, with strong documentation skills and attention to detail.

Qualifications

• Minimum hands-on QC laboratory experience with analytical data review.
• Experience with IPQA activities and batch documentation review.

Responsibilities

• Perform IPQA activities for tablets, external liquids and topical preparations.
• Conduct in-process and finished-product quality checks.
• Review batch documentation and batch release activities.
• Support process validation and line clearance to ensure GMP/GDP compliance.

Skills

QC Documentation and Analytical Data

Analytical report review

Attention to detail

Documentation practices

GMP/GDP awareness

Tools

Potentiometer Metrohm

GC (Gas Chromatography)

Polarimeter

TOC Analyzer

Dissolution Test Apparatus

Job description

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.