- **Formulation Development:** Design and develop innovative pharmaceutical formulations (solid, liquid, semi-solid, etc.) in accordance with project objectives and timelines.
- **Process Development:** Optimize and scale-up formulation processes from lab-scale to pilot and commercial-scale manufacturing.
- **Experimental Design:** Plan, execute, and analyze experiments to support formulation development and process optimization, ensuring reproducibility and robustness of results.
- **Documentation:** Prepare and review technical documents, including formulation protocols, batch records, development reports, and regulatory submission documents.
- **Collaboration:** Work closely with cross-functional teams, including Analytical Development, Quality Assurance, Regulatory Affairs, Manufacturing, Engineering and Supply chain to ensure project success.
- **Compliance:** Ensure all laboratory activities comply with regulatory requirements, Good Laboratory Practices (GLP), and Good Manufacturing Practices (GMP).
- **Innovation:** Stay current with industry trends, scientific literature, and technological advancements to drive innovation in formulation development.
- **Problem Solving:** Troubleshoot and resolve technical issues related to formulation and process development.
· Any other duties as assigned by supervisor.
Education:**
- Associate Scientist: Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related field.
- **Experience:**
Associate Scientist: 2+ years of experience in pharmaceutical formulation development or related field. Fresh graduate will be considered.
