- Conduct analytical testing of raw materials, in-process samples, and finished products to ensure compliance with quality standards.
- Develop and validate new methods for analyzing pharmaceutical products using techniques such as HPLC, GC, UV spectrophotometry, etc.
- Collaborate with cross-functional teams to resolve issues related to product quality and stability.
- Maintain accurate records of test results, protocols, and reports in accordance with regulatory requirements.
Job Requirements :
- Bachelor's degree in Chemistry or a related field (BSc).
- 0-1 year of experience in Analytical Research Development or In Process Quality Assurance (IPQA) department.
- Solid understanding of analytical method development principles and validation procedures.
- Familiarity with Good Laboratory Practices (GLP) guidelines.