Senior Officer Quality Control (QC)

Fairdeal Corporation (FDC); Goa; On-site; INR 600,000 - 1,100,000; Full time

Job summary

FDC Limited, Goa Unit III in Verna, is seeking a Senior Officer QC Stability Analyst to perform stability and routine quality control analytics on finished products and raw materials. The role involves operating HPLC/UPLC/UV methods, conducting dissolution and related physical tests, and maintaining GLP-compliant records while supporting audits and investigations.

The position requires meticulous documentation, instrument calibration verification, and collaboration with cross-functional teams to

Qualifications

• Stability testing experience.
• Quality control analytics for finished products and raw materials.
• Experience following cGMP and GLP.
• Data integrity and accurate record keeping.

Responsibilities

• Perform stability, finished product and raw material analyses as per SOPs.
• Use HPLC, UPLC and UV spectrophotometry; conduct dissolution, hardness, friability, disintegration tests.
• Verify instrument calibration and maintain standards and reagents.
• Prepare standard solutions and maintain records in worksheets and LIMS.
• Contribute to investigations of OOS/OOT results and deviations; support audits.

Tools

HPLC

UPLC

UV Spectrophotometry

Dissolution testing

pH meter

Conductivity meter

Balances

Job description

Senior Officer QC Stability Analyst
FDC Limited | Goa Unit III, Verna

The role focuses on stability sample testing and also supports routine quality control analysis of finished products and raw materials.

Key Responsibilities

• Perform physical and chemical analysis of stability, finished product and raw material samples in accordance with approved specifications, SOPs and regulatory requirements. Perform rinse and swab sample analysis.
• Conduct testing using HPLC, UPLC and UV spectrophotometry, along with dissolution, hardness, friability and disintegration testing.
• Perform daily verification of pH meters, conductivity meters and balances. Confirm instrument calibration status before analysis and use valid reference standards, working standards and chemicals.
• Prepare and standardize volumetric solutions, prepare reagents and indicators, and maintain the associated records.
• Record analytical data at the time of work in approved worksheets, logbooks and LIMS. Maintain complete and accurate records in line with cGMP, Good Laboratory Practices (GLP) and data integrity requirements.
• Participate in investigations of out-of-specification (OOS) and out-of-trend (OOT) results, deviations and analytical incidents. Conduct hypothesis testing as part of root cause investigations.
• Maintain current QC documents and GLP records, revise documents through change control, and support internal and external audits, including responding to auditor queries within the scope of assigned work.
• Maintain the QC laboratory, coordinate with other departments or sites as needed, and carry out additional QC duties assigned by the supervisor.