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Job Description
- Method Development and Optimization: design and optimize analytical methods for the characterization, identification, and quantification of pharmaceutical products.
- Validation of analytical method: establish and validate robust analytical methods to ensure the quality, purity, and potency of pharmaceutical products.
- Preparing of NODCAR files.
- Ensure compliance with relevant regulatory requirements and guidelines.
- Conducting the comparative dissolution studies.
- Analysis of R&D trials.
- Implementation the high-quality standards and GLP requirements.
Job Requirements
- Bachelor's degree of pharmacy or science (chemistry).
- 3-5 years of experience in similar position (males are preferred).
- Strong knowledge of development processes, regulations, and quality control practices is essential.
- Familiarity with regulatory guidelines such as (FDA) and (ICH) guidelines (is important).
- Proficiency in a wide range of analytical instruments commonly used in the pharma industry like (HPLC, GC, UV-Vis, and dissolution tester).
- Experience with method development, validation, and transfer.
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