- RESPONSIBILITIES AND TASKS:
- Responsible for accurate sampling of Stability product according to QC procedures and ICH guidelines.
- Responsible to perform all physical and chemical checks on Stability products according to QC specifications.
- Responsible to fill the required Quality Reports which contains detailed information on the performed tests and calculations according to the supplied specifications.
- Responsible to apply GLP, GDP.
- Responsible to exactly follow QC policies, standards, and procedures.
- Responsible for create protocol, Report & COA of the stability study.
- Responsible to receive and enter & withdraw stability samples & preparation.
- Perform Comparative dissolution study, create Protocol & Final Report.
- Respond to the EDA comments & Preparation technical File.
- Participating in Method Development & Analytical method validation study. Preparation Protocol & Final report.
- Follow-up development of the method of analysis of new drug molecules suitable for routine work of QC.
- Development of stability-indicating assay of pharmaceutical products.
- The validation of all the developed methods of analysis.
- Solving any problems encountered in all the developed methods of analysis.
- Documentation of MOA, Specs & work sheet.
Proven work experience as a Physicist or similar roleStrong aptitude for mathematics, calculus, and trigonometryExcellent verbal and written communication skillsExceptional presentation and reporting abilitiesEnthusiastic and passionate about physicsRelevant training and/or certifications as a Physicist