- 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

Benefits

- Commuter assistance

- Versatile 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)
🏢 ASPIRIT VISION SOLUTION
📍 Roorkee