Quality Control Associate

Key Responsibilities:

Perform analysis of raw materials, in-process samples, and finished products as per approved specifications, test methods, and protocols.
Operate, calibrate, and maintain analytical instruments including HPLC, FTIR, and GC.
Troubleshoot analytical instruments, particularly HPLC systems, and ensure uninterrupted laboratory operations.
Ensure proper documentation and data integrity in compliance with GMP and GLP guidelines.
Maintain and update laboratory records, test reports, calibration records, logbooks, and analytical worksheets.
Utilize server-based chromatography software for data acquisition, processing, and reporting for HPLC and GC systems.
Ensure compliance with Good Documentation Practices (GDP) at all times.
Coordinate with QA for out-of-specification (OOS) investigations, deviations, and corrective actions when required.
Ensure proper handling, labeling, storage, and disposal of samples and chemicals.
Support internal and external audits by providing required documentation and technical explanations.

Technical Skills & Knowledge:

Strong operating knowledge of HPLC, FTIR, and GC instruments.
Hands-on experience in calibration, operation, and troubleshooting of HPLC systems.
Knowledge of SAP for material management, data entry, or quality-related transactions.
Proficiency in MS Office applications (Word, Excel, PowerPoint).
Experience working with server-based chromatography software for HPLC and GC.
Understanding of GMP, GLP, GDP, and regulatory compliance requirements.

Educational Qualification:

B.Sc / M.Sc in Chemistry / Analytical Chemistry / Pharmaceutical Sciences or equivalent.

Experience:

1–4 years of relevant experience in a QC laboratory within pharmaceutical / medical device / chemical manufacturing industries.