Key Responsibilities

- Analytical Testing: Performing wet chemistry and instrumental analysis (HPLC, GC, UV-Vis) on raw materials, intermediates, packaging, and finished products.
- Documentation & Compliance: Preparing, reviewing, and managing SOPs, batch records, stability protocols, and reports, ensuring adherence to Positive Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
- Equipment Management: Calibrating, maintaining, and troubleshooting lab instruments like HPLC systems.
- Data Integrity: Ensuring accuracy and integrity of all analytical data, including audit trail reviews.
- Deviation Management: Investigating Out-of-Specification (OOS) results, preparing deviation reports, and implementing Corrective and Preventive Actions (CAPA).
- Stability Studies: Preparing and monitoring stability study samples and reporting trends.
- Material Release: Participating in the decision to release or reject raw materials, intermediates, and finished products.

Minimum Exp. - 3 Years EQ_ B.Pharma

Job Type: Permanent

Pay: ₹300,000.00 - ₹500,000.00 per year

Benefits

- Food provided
- Health insurance
- Paid sick time
- Paid time off
- Provident Fund

📌 QC Officer(Pharmaceutical Industry) (Ghaziabad)
🏢 ALBERT DAVID
📍 Ghaziabad