A leading pharmaceutical company in Ahmedabad, Gujarat, is hiring for the Officer, QC Documentation position. The company specializes in quality-driven drug manufacturing with a strong focus on regulatory compliance (GMP, GLP) and advanced analytical testing.
Detailed Job Description
Key Responsibilities:
✔ Instrument Handling: Operate & maintain HPLC, UV, FTIR, GC, Polarimeter, KF, Auto-titrator
✔ QMS Documentation: Manage OOS, OOAL, Deviations, Change Controls, Incidents, CAPA
✔ Data Review: Verify logbooks, raw data (RM, PM, finished products, water analysis)
✔ SOP Compliance: Ensure adherence to GLP, Data Integrity, Regulatory Standards
✔ LIMS & QMS: Maintain electronic records, investigations, and reports
Required Skills:
- Analytical Instrumentation (HPLC, GC, UV, FTIR) – Practitioner
- GLP & Documentation Accuracy – Practitioner
- Data Integrity & Compliance – Practitioner
- OOS/OOT/Deviation Handling – Beginner to Practitioner
- LIMS & QMS Software – Working Knowledge
Eligibility & Qualifications
✅ Education: Bachelor’s Degree in Pharmacy, Chemistry, or related field
✅ Experience: 1-4 years in QC/QMS documentation (Pharma/Biotech)
✅ Internal Candidates: Must have completed 2 years in current role
Benefits & Work Culture
🔹 Stable Career Growth in a GMP-compliant environment
🔹 Hands-on Experience with advanced lab instruments
🔹 Professional Development in QMS & Regulatory Compliance
🔹 Competitive Salary + Health Benefits
How to Apply
📅 Last Date: August 1, 2025
📍 Location: Sanand, Ahmedabad, Gujarat
