Caplin One, part of Caplin Point Laboratories, is committed to delivering quality and compliance in the pharmaceutical industry. We specialize in providing high-quality products with a strong focus on regulatory standards, ensuring safety, efficacy, and reliability. Join us and be part of a team dedicated to excellence!

Key Responsibilities of the Quality Control Analyst

As a Quality Control Analyst, you will play a vital role in ensuring that all products meet rigorous quality standards. Responsibilities include:

• Analysis and Reporting: Conducting thorough analysis and reporting of raw materials, in-process materials, and finished products as per Standard Test Procedures (STPs).
• Method Verification and Validation: Performing method verification, validation, and transfer to support accurate quality control.
• Instrument Operation: Ensuring proper usage of laboratory instruments in line with SOPs, including handling and maintenance of records.
• Compliance: Adhering to Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Good Documentation Practice (GDP) standards.
• Reporting: Promptly reporting any out-of-specification or out-of-trend results to the Quality Control Manager for review.

Preferred Skills and Experience

The ideal candidate will have experience in the following areas:

• Experience Level: 0–4 years in Quality Control or a related role.
• Technical Skills: Proficiency in HPLC/GC analysis, LIMS software handling, instrument operation and calibration, and chemical analysis.
• Regulatory Compliance: Knowledge of GMP, GLP, and GDP compliance standards.

Location and Number of Positions Available

• Location: Kakkalur Plant, Thiruvallur
• Positions Available: 10 Quality Control Analyst roles

How to Apply

If you’re ready to join Caplin One’s team, send your CV to amudhan.g@caplinpoint.net. Don’t miss this opportunity to advance your career in pharmaceutical quality control with a reputable industry leader!