Quality Control

We are seeking motivated, detail-oriented QC Analysts to join our Pharmaceutical Analytics team. The successful candidates will contribute to ensuring the quality, safety, and efficacy of our pharmaceutical products through rigorous analytical testing and adherence to regulatory requirements. This is a walk-in interview position, suitable for fresh graduates as well as experienced professionals.

Key Responsibilities:

• Perform quantitative and qualitative analysis of pharmaceutical raw materials, in-process samples, finished products, and stability samples using:
• High-Performance Liquid Chromatography (HPLC)
• Gas Chromatography (GC)
• Infrared Spectroscopy (IR) (FTIR/NIR as applicable)
• Dissolution testing using USP apparatus (e.g., USP Apparatus I and II)
• Develop, validate, and transfer analytical methods in accordance with ICH guidelines, GMP, and company SOPs.
• Prepare, standardize, and calibrate analytical instruments; maintain instrument logs and daily QC check routines.
• Analyze data, prepare clear and accurate analytical reports, and review results for accuracy and compliance.
• Investigate out-of-specification (OOS) and out-of-trend (OOT) results; initiate CAPAs as required.
• Ensure proper sample handling, labeling, storage, and chain-of-custody procedures.
• Maintain GMP documentation, SOPs, method files, and integrity of data systems (LIMS/CDS).
• Monitor and document instrument maintenance, preventive maintenance (PM), and calibration activities.
• Collaborate with R&D, Manufacturing, and Quality Assurance to support product releases and regulatory submissions.
• Adhere to health, safety, and environmental policies; participate in safety drills and audits as needed