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 Valuable Manufacturing Practices (GMP) and Positive 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

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

📌 Qc Officer Pharmaceutical Industry Ghaziabad
🏢 Albert David
📍 Ghaziabad