Downstream Production

Roles and Responsibilities :

• Conduct analytical testing of pharmaceutical products using techniques such as HPLC, GC, and UV spectroscopy.
• Develop and validate methods for the analysis of raw materials, intermediates, and finished products to ensure compliance with regulatory requirements.
• Collaborate with cross-functional teams to troubleshoot issues related to product quality and stability.
• Maintain accurate records of test results, protocols, and reports in accordance with cGMP guidelines.

Job Requirements :

• 1-5 years of experience in a laboratory setting within the pharmaceutical industry.
• Strong understanding of chromatography (HPLC), purification techniques (e.g., filtration), and spectroscopic methods (UV).
• Familiarity with Good Laboratory Practices (cGMP) regulations and current Good Manufacturing Practices (cGMP).
• Bachelor's degree in Chemistry or related field; Master's degree preferred.