Managing Stability Studies: Designing and executing long-term, accelerated, and intermediate stability protocols according to ICH guidelin
Sample Management: Pulling, preparing, and charging stability samples from designated climatic chambers at specific, predetermined time intervals
Analytical Testing: Performing physical, chemical, and chromatographic tests (such as HPLC assays and dissolution) to detect degradation products or potency shifts.
Chamber Monitoring: Tracking and maintaining temperature and relative humidity inside stability walk-in rooms or reach-in chambers.
Data Documentation: Recording analytical data accurately, compiling stability reports, and ensuring strict data integrity.
OOS/OOT Investigation: Identifying, logging,



and investigating any Out-of-Specification (OOS) or Out-of-Trend (OOT) results.
Regulatory Compliance: Aligning all procedures with cGMP guidelines to support shelf-life claims and regulatory filings.

Pay: ₹25,000.00 - ₹35,000.00 per month

Perks:
Commuter assistance
Adaptable schedule
Health insurance
Internet reimbursement
Leave encashment
Life insurance
Paid sick time
Provident Fund

Education:
Bachelor's (Required)

Experience:
Qc: 3 years (Required)

Work Location: In person

📌 Qc Stability Pharma Background Roorkee (India)
🏢 ASPIRIT VISION SOLUTION
📍 India