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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:
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- 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!
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