Job description:

• Preparation of specifications and development of analytical methods for testing new products, new APIs and intermediates.
• Preparation of protocols for method validation.
• Conducting tests for analytical method validation based on the protocol.
• Preparation of analytical method validation report.
• Testing of research samples of drug product according to stability protocol, new APIs and intermediates.
• Reporting the results.
• Performance of dissolution profiles for in vitro dissolution study and preparation of in-vitro study report.
• Write quality part of the dossier.

Job requirement:

• Bachelor’s degree or higher degree from Pharmacy, Chemistry or similar.
• At least 2- 3 years of relevant experience in analytical R&D or quality control department of pharmaceutical products.
• Be able to analyze samples by analytical techniques like HPLC, UV-Vis, dissolution tester and others.
• Has knowledge of validation of analytical methods and development of analytical methods.
• Be able to write quality part of registration dossier.
• Preferred to have experience in managing analytical laboratory equipment.
• Ability to read and write technical English; able to communicate in English.

Please contact our Recruiter or apply via email recruitment@davipharm.info