AddressJob Responsibilities:
The candidate will be responsible for the dose formulation analysis for preclinical studies. He/She is expected to drive technical innovation in formulation method development and involved in validation, analysis of preclinical dosing formulations as per the regulatory guidelines.
1. Assure that all the development and validation of analytical method for formulation activities are documented as per GLP regulations and company procedures.
2. Responsible for analysis of dosing formulation using Waters Alliance HPLC system and operation, calibration and maintenance of HPLC/UPLC.
3. To work as per OECD GLP/cGMP and to ensure its compliance.
4. Calibration of other laboratory instruments, inventory managements. Communication with external agencies for calibration of instruments.
5. As needed design and execute formulation trials, analytical testing and evaluate stability data to finalize formulation composition for preclinical toxicity studies.
Requirement:
- Around 5-6 years of experience in Preclinical dose formulation analysis under regulated and GLP environment.
- Hands on experience on waters HPLC/UPLC with Empower software.
- Provide recommendations for continuous improvements in practices and systems to improve performance and enhance efficiency and quality.
Sun Pharma Advanced Research Company Ltd is looking for .
Education : Any Graduate / Post Graduate
