Senior Scientist, Drug Product & Stability
On-siteVictoria, Central and Western, Hong Kong
Job Summary
Define formulation, drug product process, and stability development strategies aligned with portfolio objectives. Act as a technical subject matter expert in biologics, designing and executing stability, container closure, and robustness studies while applying Quality by Design principles. Lead ICH-compliant GMP stability programs, manage technology transfers, and generate CMC insights for regulatory submissions. Collaborate with cross-functional teams globally to drive innovation through automation and AI-enabled approaches, providing technical leadership and mentorship. Based at CSL Melbourne in a newly created team.
Required Qualifications
- A tertiary qualification in Pharmaceutical Sciences, Chemistry, Biochemistry, Biotechnology, Chemical Engineering or a related discipline
- PhD or equivalent industry experience
- 3+ years of experience in formulation development, stability and/or drug product process development within a regulated biopharmaceutical industry environment
- Strong technical leadership capability with a proven ability to define scientific direction and prioritise critical deliverables
- Experience working effectively within cross-functional global organisations
- Excellent written and verbal communication skills, including the ability to translate complex ideas
- Scientific curiosity and a passion for solving complex challenges in biologics development
- A growth mindset, strong learning agility and a collaborative approach to teamwork and scientific problem-solving within a research environment
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