Your work will include analytical method development, solubility testing, sterilisation studies, container closure compatibility, sample preparation, and basic analytical testing. You will work closely with the wider development team to generate experimental data to support IND submission.
Key Responsibilities:
- Perform formulation development and optimization studies.
- Conduct solubility, stability, and container closure compatibility studies.
- Support outsourced sterilisation feasibility studies, including autoclaving, gamma irradiation, and sterile filtration.
- Evaluate the impact of formulation and sterilisation conditions on product quality.
- Support with analytical testing.
- Prepare study protocols, technical summaries, and experimental reports.
- Collaborate closely with internal cross-functional teams and external CDMOs to coordinate studies and ensure successful execution.