QC Officer(Pharmaceutical Industry)

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 Good 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