CSL1 follower17 jobs

Principal Scientist, Pathogen Safety

SeniorFull-timeHybrid655 Elizabeth St, Melbourne VIC 3000, AustraliaProfessional servicesPosted 1 week agoVerified 1 week ago
Pending fitX of Y criteria met

About the job

The Principal Scientist, Pathogen Safety Support is a vital job that provides scientific and operational expertise to enhance pathogen safety activities across manufacturing, technical operations, and product lifecycle management. This position plays a crucial role in assessing pathogen safety risks, supporting regulatory and compliance obligations, and contributing to projects that ensure the safety, quality, and supply of CSL products. The team thrives on collaboration, continuous improvement, and a commitment to compliance excellence, making it an exciting environment for growth and innovation.

Meet the team

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Think you're a good fit?See what the hiring team are looking for

You'll be responsible for

🛠️

Planning and executing scientific work packages

Plan and execute scientific work packages supporting pathogen safety activities across the product lifecycle.
⚖️

Conducting scientific risk assessments

Conduct scientific risk assessments related to manufacturing changes, deviations, product complaints, and other operational matters.
🌐

Collaborating with cross-functional teams

Collaborate with Manufacturing Sciences & Technology, Technical Operations, Quality, and Regulatory Affairs to assess and prioritize pathogen safety requests.

Key criteria

🔬

Scientific expertise in pathogen safety

Strong background in pathogen safety and related scientific disciplines.

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📊

5+ years in biopharmaceutical industry

Demonstrated experience in biopharmaceutical, biotechnology, or life sciences.

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🤝

Cross-functional collaboration skills

Proven ability to work effectively across diverse teams and stakeholders.

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A meaningful career starts with a match

View your fit

5 criteria for this job
Scientific expertise in pathogen safety
Strong background in pathogen safety and related scientific disciplines.

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5+ years in biopharmaceutical industry
Demonstrated experience in biopharmaceutical, biotechnology, or life sciences.

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Cross-functional collaboration skills
Proven ability to work effectively across diverse teams and stakeholders.

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Technical document authoring experience
Experience writing and reviewing regulatory submissions and technical documents.

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Analytical and problem-solving skills
Strong capabilities in risk assessment and technical issue resolution.

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