Job Summary :
We are seeking a skilled and experienced QC Scientist to support the manufacturing of pharmaceutical products. The primary responsibilities include routine testing and analysis of finished products (tablets, capsules, sub-gels) and raw materials, utilizing a variety of laboratory instruments and techniques.
Key Responsibilities :
- Conduct routine analysis of finished products and raw materials, including weight, chemistry tests for raw materials, and stability sample testing under different ICH conditions.
- Operate and troubleshoot laboratory instruments such as HPLC, GC, Karl Fischer, FTIR
- Experience with chromatography software (e.g., Empower 3) is highly preferred.
- Follow approved testing procedures and methods according to internal SOPs and USP monographs. Report data accurately and promptly.
- Participate in laboratory investigations using TrackWise or MasterControl software.
- Support routine lab activities such as balance calibration and pH calculations
- Perform stability testing of pharmaceutical products and excipients under ICH conditions
Position Requirements :
4-8 years of hands-on experience in a laboratory setting, with a focus on oral solid dosage forms (tablets, capsules, sub-gels) and raw materials.Expert in dissolution and stability testing and compliance with USP standards.Experience with laboratory instrumentation such as HPLC, GC, Karl FischerPrior experience with Empower 3 software or similar chromatography software is a significant advantage.Knowledge of investigations processes, trending, and documentation of test results.Ability to adhere to SOPs, USP monographs, and GMP regulations