Job Description

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: ?250,000.00 - ?500,000.00 per year

Benefits:

Food provided Health insurance Paid sick time Paid time off Provident Fund
Expected Start Date: 15/12/2025