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About the role
Key responsibilities & impact- Provide scientific expertise to support pathogen safety activities across manufacturing, Technical Operations, product development, and lifecycle management.
- Perform scientific evaluations and pathogen safety risk assessments related to manufacturing changes, deviations, investigations, product complaints, and process improvements.
- Prepare and review scientific documentation including technical reports, regulatory responses, risk assessments, and supporting documentation.
- Contribute scientific expertise to cross-functional Technical Operations and product development projects on local and global level.
- Support investigations and resolve scientific questions impacting pathogen safety activities, e.g., virus reduction unit operations, emerging pathogens, or raw material safety.
- Represent the Global Pathogen Safety function within multidisciplinary project teams.
- Collaborate with Manufacturing Sciences & Technology (MS&T), Quality, Regulatory Affairs, Process Development, Manufacturing, and other technical functions.
- Provide timely scientific input to support project objectives and business priorities.
- Communicate technical findings clearly to both scientific and non-scientific stakeholders.
- Identify opportunities to improve scientific processes, workflows, and knowledge sharing.
- Support implementation of best practices and continuous improvement initiatives within Pathogen Safety.
- Contribute to maintaining scientific standards and operational excellence.
- Ensure all activities comply with applicable regulatory requirements, quality standards, and internal procedures.
- Support inspections, audits, and regulatory interactions as required.
- Maintain high standards of scientific integrity, documentation, and data quality.
Requirements
What you’ll need- Master’s degree (MSc) or PhD in Virology, Microbiology, Biotechnology, Biology, Biochemistry, or another relevant Life Sciences discipline.
- Approximately 3–5 years of relevant experience within the biopharmaceutical, biotechnology, vaccine, or life sciences industry.
- Experience supporting manufacturing, Technical Operations, process development, or product lifecycle activities.
- Experience working in cross-functional project teams.
- Knowledge of GxP-regulated environments is advantageous.
- Scientific expertise in virology, microbiology, pathogen safety, biotechnology, or related disciplines.
- Strong analytical thinking and scientific problem-solving skills.
- Experience performing scientific risk assessments and interpreting technical data.
- Ability to communicate complex scientific concepts clearly.
- Strong collaboration and stakeholder management skills.
- Ability to manage multiple priorities in a dynamic, global environment.
- Excellent written and spoken English.
Benefits
Comp & perks- For more information on CSL benefits visit How CSL Supports Your Well-being | CSL
ATS Keywords
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Hard Skills & Tools
Scientific EvaluationsTechnical Documentation PreparationRisk Assessment InterpretationProcess Development SupportManufacturing Change Evaluation
Soft Skills
Strong CollaborationStakeholder ManagementAnalytical Problem-SolvingEffective Communication
Certifications
Master’s Degree (MSc) or PhD in Relevant Life Sciences